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1 - Analytical R&D : Scientist

Job title: Analytical R&D : Scientist

Job Description:

  1. Performing analytical method validation/ raw material/ finished product analysis
  2. Performing assay by using HPLC
  3. To perform analysis related to Method Transfer and Analytical Method Verification
  4. Preparing method validation protocols & reporting.

Required Candidate profile:

Education : M.Sc / M. Pharma / Ph.D

Experience : 2 - 8 years

Position : Research Associate to Research Scientist

Location : Hyderabad

Industry Type : Pharmaceutical

Functional Area : R&D, Pharmaceuticals

Employment Type : Full Time

Forward your CV / Resume : careers@cellixbio.com

About Cellix bio:

Cellix Bio employees and teams apply sound science to develop and deliver medicines that focus on unmet medical needs around the world. Our current prescription products at various stages of development target to serve patients across therapeutic areas including metabolism, immunology, infectious diseases, neuroscience, ophthalmology, and oncology.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. You will help make an impact on people’s lives and change futures every day. We are equally committed to bringing out your best and fostering a collaborative workplace built on trust and respect.

We empower our people to take charge of their potential. We offer training and leadership development programs tailored to help you build valuable skills and succeed in your career. As you discover your potential, your professional and personal future will become brighter.

What do we do?

Founded in 2014, we are the leading drug discovery and development company. We generate our own drug design data before combining the critical power of AI with the creativity of involving proprietary platform technology, Synergix AITM and expertise of our world-class scientists. This allows us to shorten the pre-clinical drug discovery stage and, in turn, substantially accelerate the delivery of new treatments to patients worldwide. By reducing the number of compounds analysed, we aim to vividly reduce the time and cost of discovering and developing new medicines. Cellix Bio balances Synergix AITM plus human creativity in the drug discovery.

Our targeted discovery process enables the creation of new markets and solutions to both old and new problems. Driven by the speed and accuracy of our platform, Synergix AITM accomplishes in months what previously took years, saving tens of millions in research and development costs. Each of our lead candidates are unique with powerful therapeutic benefits. The molecular entities that we discover are the first of their kind and patented.

Using our Synergix AITM drug discovery platform and the insights from our successful drug development and clinical data, we can identify synergistic pharmacology between bio-actives, combining them to address disease related biochemical pathways and targets. However the rubrics of drug discovery are very complex - not all are known and some are not readily describable as a restricted set of moves.

2 - EXECUTIVE PURCHASE

Job title: EXECUTIVE PURCHASE

Location: Hyderabad, India - 1 opening

Qualification

  1. Master’s or Bachelor’s degree in Science / Pharmacy / Commerce
  2. At least 5 years’ experience in similar function in pharmaceutical industry (Especially Finished dosage forms)

Skills Required

  1. Strong initiative skills, working both independently and as part of a team
  2. Clear-cut proficiency in English communication
  3. Advanced Microsoft office skills (Word, Excel, PowerPoint and Outlook)

Change more than just your career:

People at PharmSol are thinkers and doers. That’s why we recruit people with more than just a passion for pharmaceutical solutions – they must also have the courage to bring them to life. There are so many opportunities available – from providing advice, information and solutions to implementing it in pharma plants that make a positive difference for our clients. We build our firm with an entrepreneurial spirit, fueled by dynamic teamwork and collaboration, and founded on trust and respect for each other. The opportunities are endless – the choice is yours.

The Company Overview:

PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.

Since its inception 18 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.

Today, PharmSol has earned a worldwide reputation for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavour to bring new products to the market and implement new ideas & technologies to meet needs of the future.

PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal deliverance on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.

PharmSol has widened its niche, by providing on a supplemental or comprehensive basis, fully tailored solutions for meeting the Product Development, IPR, Facility Design, Compliance, Registrations, Market Access, Audits and Supply Chain requirements, with a focus on EU, US, TGA, WHO and other International Regulatory Requirements.

PharmSol continues to strive for excellence and achieve its goal to forever be the leader in pharma and the foremost choice for its customers. Its visionary leadership, with nearly 40 years of success, continues to innovate and grow, through cementing its presence in Africa and far east Asia as well as through new ventures, such as Eminus eGlobal Institute, which are destined to transform the pharma industry.

explore our site for more jobs in Hyderabad

3 - Executive Quality Affairs

Job title: Executive Quality Affairs

Location: Hyderabad, India - 2 openings

Qualification:

  1. Master’s or Bachelor’s degree in Science / Pharmacy
  2. At least 5 years’ experience in similar function in pharmaceutical industry (Especially Finished dosage forms)

Skills Required

  1. Candidate should be from QA / QC background
  2. Sound and deep knowledge in to current GMP requirements (US FDA, EU GMP, PIC/s)
  3. Clear understanding of QA system and principles
  4. Strong initiative skills, working both independently and as part of a team
  5. Clear-cut proficiency in English communication
  6. Advanced Microsoft office skills (Word, Excel, PowerPoint and Outlook)

Change more than just your career:

People at PharmSol are thinkers and doers. That’s why we recruit people with more than just a passion for pharmaceutical solutions – they must also have the courage to bring them to life. There are so many opportunities available – from providing advice, information and solutions to implementing it in pharma plants that make a positive difference for our clients. We build our firm with an entrepreneurial spirit, fueled by dynamic teamwork and collaboration, and founded on trust and respect for each other. The opportunities are endless – the choice is yours.

The Company Overview:

PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.

Since its inception 18 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.

Today, PharmSol has earned a worldwide reputation for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavour to bring new products to the market and implement new ideas & technologies to meet needs of the future.

PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal deliverance on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.

PharmSol has widened its niche, by providing on a supplemental or comprehensive basis, fully tailored solutions for meeting the Product Development, IPR, Facility Design, Compliance, Registrations, Market Access, Audits and Supply Chain requirements, with a focus on EU, US, TGA, WHO and other International Regulatory Requirements.

PharmSol continues to strive for excellence and achieve its goal to forever be the leader in pharma and the foremost choice for its customers. Its visionary leadership, with nearly 40 years of success, continues to innovate and grow, through cementing its presence in Africa and far east Asia as well as through new ventures, such as Eminus eGlobal Institute, which are destined to transform the pharma industry.

explore our site for more jobs in Hyderabad

4 - EXECUTIVE QUALITY CONTROL

Job title: EXECUTIVE QUALITY CONTROL

Location: Hyderabad, India - 1 opening

Qualification:

  1. Master’s or Bachelor’s degree in Science / Pharmacy
  2. At least 5 years’ experience in similar function in pharmaceutical industry (Especially Finished dosage forms) Skills Required:
  3. Candidate should be from ARD/QC background
  4. Sound and deep knowledge in to current GMP requirements (US FDA, EU GMP, PIC/S)
  5. Clear understanding of GLP system and principles
  6. Strong initiative skills, working both independently and as part of a team
  7. Clear-cut proficiency in English communication
  8. Advanced Microsoft office skills (Word, Excel, PowerPoint and Outlook)

Change more than just your career:

People at PharmSol are thinkers and doers. That’s why we recruit people with more than just a passion for pharmaceutical solutions – they must also have the courage to bring them to life. There are so many opportunities available – from providing advice, information and solutions to implementing it in pharma plants that make a positive difference for our clients. We build our firm with an entrepreneurial spirit, fueled by dynamic teamwork and collaboration, and founded on trust and respect for each other. The opportunities are endless – the choice is yours.

The Company Overview:

PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.

Since its inception 18 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.

Today, PharmSol has earned a worldwide reputation for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavour to bring new products to the market and implement new ideas & technologies to meet needs of the future.

PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal deliverance on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.

PharmSol has widened its niche, by providing on a supplemental or comprehensive basis, fully tailored solutions for meeting the Product Development, IPR, Facility Design, Compliance, Registrations, Market Access, Audits and Supply Chain requirements, with a focus on EU, US, TGA, WHO and other International Regulatory Requirements.

PharmSol continues to strive for excellence and achieve its goal to forever be the leader in pharma and the foremost choice for its customers. Its visionary leadership, with nearly 40 years of success, continues to innovate and grow, through cementing its presence in Africa and far east Asia as well as through new ventures, such as Eminus eGlobal Institute, which are destined to transform the pharma industry.

explore our site for more jobs in Hyderabad

5 - EXECUTIVE REGULATORY AFFAIRS

Job title: EXECUTIVE REGULATORY AFFAIRS

Location: Hyderabad, India - 1 opening

Qualification:

  1. Master’s or Bachelor’s degree in Science / Pharmacy
  2. At least 7-10 years’ experience in similar function in pharmaceutical industry Skills Required:
  3. Candidate should be from RA having supported regulatory affairs function on finished dosage form
  4. Sound and deep knowledge in to current Regulatory / GMP requirements (US FDA, EU GMP, PIC/s )
  5. Strong initiative skills, working both independently and as part of a team
  6. Clear-cut proficiency in English communication
  7. Advanced Microsoft office skills (Word, Excel, PowerPoint and Outlook)

Change more than just your career:

People at PharmSol are thinkers and doers. That’s why we recruit people with more than just a passion for pharmaceutical solutions – they must also have the courage to bring them to life. There are so many opportunities available – from providing advice, information and solutions to implementing it in pharma plants that make a positive difference for our clients. We build our firm with an entrepreneurial spirit, fueled by dynamic teamwork and collaboration, and founded on trust and respect for each other. The opportunities are endless – the choice is yours.

The Company Overview:

PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.

Since its inception 18 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.

Today, PharmSol has earned a worldwide reputation for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavour to bring new products to the market and implement new ideas & technologies to meet needs of the future.

PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal deliverance on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.

PharmSol has widened its niche, by providing on a supplemental or comprehensive basis, fully tailored solutions for meeting the Product Development, IPR, Facility Design, Compliance, Registrations, Market Access, Audits and Supply Chain requirements, with a focus on EU, US, TGA, WHO and other International Regulatory Requirements.

PharmSol continues to strive for excellence and achieve its goal to forever be the leader in pharma and the foremost choice for its customers. Its visionary leadership, with nearly 40 years of success, continues to innovate and grow, through cementing its presence in Africa and far east Asia as well as through new ventures, such as Eminus eGlobal Institute, which are destined to transform the pharma industry.

explore our site for more jobs in Hyderabad

6 - Formulation R&D Scientist : Pharma

Job title: Formulation R&D Scientist : Pharma

Forward your CV / Resume : careers@cellixbio.com

Job Description:

R&D Scientist - Formulation Scientist

Pharmaceuticals/ Biotechnology/ Clinical Research

Required Candidate profile:

Education : Doctorate / Masters in Pharmaceutics, Pharmaceutical Chemistry, Industrial Pharmacy, Analytical Chemistry, Pharmaceutical Chemistry, Organic Chemistry or Medicinal Chemistry.

Experience : 5 - 10 Years

Position : Research Associate to Research Scientist

Location : Hyderabad

EXPERIENCE :

  1. In-depth understanding of physical pharmacy, physical chemistry, thermodynamics, chemical reaction kinetics is a must.
  2. In-depth understanding of various pre- formulation and formulation studies including excipient compatibility, forced degradation studies and unit steps in formulation manufacture is a must.
  3. Experience with pilot-scale and manufacturing-scale equipment is a plus.
  4. Experience with process analytical technologies (PAT) is a plus.
  5. Conduct API, excipient, packaging or device characterization; excipient compatibility and forced degradation studies.
  6. Develop robust lab-scale, pilot-scale and commercial-scale manufacturing process based on Quality by Design (QbD) principles using design of experiments (DOE). Recommend stage appropriate acceptance criteria. Utilize PAT where feasible. Utilize relevant statistical tools, as required.
  7. Review and analyze relevant stability data from lab-scale, pilot-scale and commercial-scale, R&D and GMP stability studies by utilizing industry standard modeling and analysis tools including regression analysis for shelf-life prediction. Develop and implement strategies to control related substances, where applicable.
  8. Draft high-quality industry standard technical documents (protocols, reports, technical memorandums, position papers etc.).
  9. Independently draft and/or review standard operating procedures (SOPs).
  10. Maintain effective and pro-active communication and coordination of activities with multi-functional stakeholders.

About Cellix bio:

Cellix Bio employees and teams apply sound science to develop and deliver medicines that focus on unmet medical needs around the world. Our current prescription products at various stages of development target to serve patients across therapeutic areas including metabolism, immunology, infectious diseases, neuroscience, ophthalmology, and oncology.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. You will help make an impact on people’s lives and change futures every day. We are equally committed to bringing out your best and fostering a collaborative workplace built on trust and respect.

We empower our people to take charge of their potential. We offer training and leadership development programs tailored to help you build valuable skills and succeed in your career. As you discover your potential, your professional and personal future will become brighter.

What do we do?

Founded in 2014, we are the leading drug discovery and development company. We generate our own drug design data before combining the critical power of AI with the creativity of involving proprietary platform technology, Synergix AITM and expertise of our world-class scientists. This allows us to shorten the pre-clinical drug discovery stage and, in turn, substantially accelerate the delivery of new treatments to patients worldwide. By reducing the number of compounds analysed, we aim to vividly reduce the time and cost of discovering and developing new medicines. Cellix Bio balances Synergix AITM plus human creativity in the drug discovery.

Our targeted discovery process enables the creation of new markets and solutions to both old and new problems. Driven by the speed and accuracy of our platform, Synergix AITM accomplishes in months what previously took years, saving tens of millions in research and development costs. Each of our lead candidates are unique with powerful therapeutic benefits. The molecular entities that we discover are the first of their kind and patented.

Using our Synergix AITM drug discovery platform and the insights from our successful drug development and clinical data, we can identify synergistic pharmacology between bio-actives, combining them to address disease related biochemical pathways and targets. However the rubrics of drug discovery are very complex - not all are known and some are not readily describable as a restricted set of moves.

7 - Microbiology Manager

If interested, please mail your resume to meenakshi@horizonbiolabs.com, admin@horizonbiolabs.com

Location: Hyderabad, Telangana

Job Summary:

We are looking for a Microbiology Manager to join our team at Horizon Biolabs Pvt Ltd in Hyderabad, Telangana. The ideal candidate will have a Master’s degree in Microbiology and a minimum of 8 years of experience in any reputed Pharma Testing Lab/CRO/Pharmaceutical Industry. As a Microbiology Manager, you will be responsible for managing and overseeing the day-to-day operations of the microbiology department, including planning and executing microbiology testing, analyzing and interpreting results, and maintaining laboratory compliance with regulatory standards.

Responsibilities:

  1. Manage and oversee the day-to-day operations of the microbiology department

  2. Plan and execute microbiology testing, including sample preparation, culture and media preparation, and analysis of results

  3. Analyze and interpret microbiology test results and prepare reports for internal and external stakeholders

  4. Maintain laboratory compliance with regulatory standards, including GLP, GMP, and ISO

5)Train and supervise microbiology technicians and ensure their compliance with laboratory protocols and safety guidelines

6)Collaborate with other departments and teams to ensure timely delivery of testing results and reports

Qualifications:

  1. Master’s degree in Microbiology or related field

  2. Minimum of 8 years of experience in any reputed Pharma Testing Lab/CRO/Pharmaceutical Industry

  3. Knowledge of microbiology testing methods, techniques, and instrumentation

  4. Experience with laboratory compliance and regulatory standards, including GLP, GMP, and ISO

  5. Strong communication and interpersonal skills

6)Ability to lead and manage a team of technicians

If you are interested in this opportunity and meet the qualifications, please apply through our website. We offer a competitive salary and benefits package, and opportunities for professional growth and development. Horizon Biolabs Pvt Ltd is an equal opportunity employer and values diversity at our company.

If interested, please mail your resume to meenakshi@horizonbiolabs.com, admin@horizonbiolabs.com

About the company:

Horizon Biolabs Pvt Ltd. is a GLP compliance Analytical Contract Research Organization located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries .

As a customer focused company , we are committed to provide quality services to meet the client requirements and are compliance with all relevant industry standards and regulations .

We have a team of dedicated scientists working on various research projects outsourced by renowned organizations for their submissions to various regulatory bodies .

Our state of the art analytical laboratory with built up area of 10,000 sq.ft . We use combinations of instruments, analytical techniques and methods to meet service needs .

8 - Product Application Specialist - Biopharma Industry

Location: Hyderabad, Telangana

Company: Avantor

Job Type: Full-time

Education: Minimum education requirement: Bachelor’s or Master’s degree in Life Sciences (Biology, Molecular Biology, Microbiology, Immunology, Biochemistry, Biotechnology, Engineering).

Experience:

  1. Minimum of 5 to 10 years industry experience in life sciences – Biopharma industry, including relevant knowledge across the workflow.

  2. Experience working with external customers within the Biotech, Biologics, Life Sciences, and/or Biopharmaceutical industries in a technical, engineering, or manufacturing capacity.

Responsibilities:

  1. Develop and execute a technical engagement strategy that is globally and cross-functionally aligned to support the positioning of Masterflex pump and tubing in customer’s process workflows for biopharma businesses.

  2. Lead as a technical expert in the biopharma industry, providing guidance and support to customers and internal teams.

  3. Collaborate with customers and internal teams to identify opportunities for product and service improvements.

  4. Deliver technical presentations and training to customers and internal teams.

  5. Provide on-site and remote technical support to customers as needed.

  6. Stay up-to-date with industry trends and developments.

Requirements:

  1. A minimum of 5 to 10 years of industry experience in the life sciences - Biopharma industry.

  2. Strong knowledge of upstream process and chromatography purification downstream process.

  3. Excellent communication, presentation, and interpersonal skills.

  4. Ability to work independently and as part of a team.

  5. Willingness to travel as needed.

If you are passionate about the biopharma industry and have the experience and skills we are looking for, we encourage you to apply for this exciting opportunity with Avantor. Apply now and take the first step towards a rewarding career with a global leader in the industry!

The job is for a Product Application Specialist for Avantor’s Fluid Handling (AFH) division in the biopharmaceutical industry. The position requires a Bachelor’s or Master’s degree in Life Sciences (Biology, Molecular Biology, Microbiology, Immunology, Biochemistry, Biotechnology, Engineering) and a minimum of 5 to 10 years of experience in the biopharma industry. The role involves providing technical guidance and support for the upstream process and chromatography purification downstream process. The specialist will be responsible for developing and executing a technical engagement strategy globally, which is aligned to support the positioning of Masterflex pump and tubing in customer’s process workflows. They will work with external and internal customers to meet business goals and maintain awareness of customers’ evolving technical challenges and material requirements. The role involves managing and prioritizing technical engagements in the field, tracking metrics related to technical customer engagements for the India sales team, and supporting the development of applications data for new and existing products and services. The successful candidate will have excellent communication and interpersonal skills and be able to develop and maintain strong technical relationships with targeted key accounts.

To apply, please click the link below:

9 - Product Specialist - Protein & Molecular Biology | Thermo Fisher Scientific | Hyderabad

Title: Product Specialist - Protein & Molecular Biology | Thermo Fisher Scientific | Hyderabad

Location: Hyderabad, Telangana

Salary: Competitive

About the Company:

Thermo Fisher Scientific is a global leader in scientific research and innovation, offering a wide range of products and services to help scientists and researchers advance their work. With a focus on protein and molecular biology, Thermo Fisher Scientific is committed to providing cutting-edge solutions to meet the needs of customers worldwide.

Job Description:

We are seeking a talented and driven Product Specialist to join our team in Hyderabad. As a Product Specialist, you will be responsible for maintaining our current customer base while actively developing new process opportunities to build a strong pipeline of projects that will fuel future growth. You will work closely with customers to understand their needs and provide solutions that meet or exceed their expectations.

Key Responsibilities:

  1. Maintain and grow existing customer relationships to maximize revenue and profitability

  2. Develop new business opportunities by identifying and targeting potential customers

  3. Provide technical support and training to customers on the use of our products

  4. Collaborate with cross-functional teams to develop and execute marketing strategies

  5. Stay up-to-date with industry trends and new product developments

Qualifications:

  1. Bachelor’s or Master’s degree in Life Sciences or a related field

  2. 3+ years of experience in a sales or business development role, preferably in the life sciences industry

  3. Strong understanding of protein and molecular biology applications and workflows

  4. Excellent communication and interpersonal skills

  5. Ability to work independently and as part of a team

To Apply:

If you are passionate about science and innovation and want to make a difference in the world, we encourage you to apply for this exciting opportunity. Please click on the link provided to submit your application. Thermo Fisher Scientific is an equal opportunity employer and welcomes diversity in the workplace.

About Thermo Fisher Scientific:

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com

10 - Scientific Writer - HEVA

Location: Hyderabad, full-time

Mission statements:

  1. Create HEVA (Health Economics and Value Assessment) Communications deliverables (including manuscripts, posters, abstracts, slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams.

  2. Manage core HEVA communication processes, templates, and products across the portfolio

  3. Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products

  4. Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes

  5. Seek opportunities to innovate HEVA value communications to increase the relevance and impact of HEVA evidence and inform optimal access and reimbursement decisions

  6. Develops and maintains TA expertise

  7. Manage end to end process through Datavision & Matrix

Collaboration:

  1. HEVA Global and Local teams
  2. RWE Global and local teams
  3. Scientific communication global or local teams
  4. Medical Information global or local teams

Duties & Responsibilities

People

  1. Maintain effectiveness relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop education and communication content as per requirement for HEVA (Health Economics and Value Assessment) Communications

  2. Interact effectively with healthcare professionals on publications content

  3. Constantly assist peer writers in developing knowledge and sharing learning

Performance:

Create HEVA (Health Economics and Value Assessment) Communications deliverables (including manuscripts, posters, abstracts, slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams as per agreed timelines and quality Process

Develop complex publications material:

  1. Act as an expert in the field of medical communication or medical information for the assigned Therapeutic area.
  2. Assist the assigned scientific communication team in conducting comprehensive publication-needs analysis
  3. Manage core HEVA communication processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with Core Value Dossier, the US AMCP dossier, and HEVA contributions as appropriate to other submissions
  4. Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products
  5. Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes
  6. Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes
  7. Implement relevant element of publication plan and associated activities for the year identified for the region
  8. Work with selected vendors within the region to deliver the required deliverables as per defined process
  9. Design an overall plan of action basis end-customers feedback & improve course content and delivery Customer

Work closely with HEVA Global and Local teams, RWE Global and local teams & scientific communication teams in regions/areas to identify publications needs and assist in developing assigned deliverables Liaise with Medical, HEVA Global and Local teams to prepare relevant & customized deliverables Knowledge, Skills & Competencies / Language

Therapy Area Exposure:

  1. Diabetes
  2. Familial hypercholesterolemia
  3. Cardiovascular disease
  4. Multiple sclerosis,
  5. Immunology
  6. Oncology
  7. Market access
  8. Emerging markets
  9. Generics
  10. Vaccines
  11. Vitamins and supplements
  12. Digestive
  13. Allergies
  14. Parkinson
  15. Haemophilia
  16. Rare diseases
  17. Rare blood diseases
  18. Stakeholder management

Project management

Publications submission

Procedures

Qualifications

Advanced degree in life sciences/ pharmacy/ similar discipline or medical degree Excellent English language knowledge Relevant training/ experience in health economics, public health, epidemiology, or other relevant health-related scientific discipline preferred Requirements of the job

2 years of experience in content creation for the pharmaceuticals / healthcare industry, or academia

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

11 - Senior Manager Products

Job title: Senior Manager Products

Location : Hyderabad, India

Qualification:

  1. Academic Qualification (minimum): B.E. / B. Tech in Mechanical / Chemical Engg. (Chem. Engg. preferred)
  2. Years of relevant professional experience: 12+ years

Skills Required:

  1. Experience as a Project Manager in pharma formulation projects involving hands on exposure to facility design & essentially spanning the FDF manufacturing categories (Solid Dosage Forms, Semi-Solid Dosage Forms, Liquid Dosage Forms, Injectable Form)
  2. In-depth knowledge w.r.t. the following project engineering disciplines for formulation projects:
    1. Process: Plant capacity calculations, Process & Utility equipment sizing; GMP requirements
    2. Mechanical: Process equipment & piping (incl. layouts) / Utilities (black & clean) / HVAC / Fire Protection (FP) & Public Health Engg. (PHE)
    3. Building Management Systems & ELV Systems
    4. Project Cost Estimation (upto + 10% accuracy level)
  3. Basic knowledge w.r.t. the following project engineering disciplines for formulation projects (Electricals [other than ELV systems], Plant Instrumentation & Automation [other than BMS], Civil Structure & Architecture)
  4. Strong exposure to project capital items procurement
  5. Exposure to & conversant with the requirements of international regulatory body (preferably EDQM, EUGMP, WHO) facility audits.
  6. Advanced knowledge on software skills: MS Office (Word, Excel & Power Point), MS Projects, AutoCad
  7. Possess profound data base w.r.t. indigenous & imported formulation process & utility equipment machinery vendors & cost.

Change more than just your career:

People at PharmSol are thinkers and doers. That’s why we recruit people with more than just a passion for pharmaceutical solutions – they must also have the courage to bring them to life. There are so many opportunities available – from providing advice, information and solutions to implementing it in pharma plants that make a positive difference for our clients. We build our firm with an entrepreneurial spirit, fueled by dynamic teamwork and collaboration, and founded on trust and respect for each other. The opportunities are endless – the choice is yours.

The Company Overview:

PharmSol, founded in 2004, has grown to become a global pharmaceutical enterprise, offering smart products and providing bespoke solutions throughout the world. PharmSol’s successful track record is credited to its team’s all round technical competence, its drive to be the leading choice for clients, its focus on building long term relationships and its longstanding dedication to prosper the pharma industry and community.

Since its inception 18 years ago, PharmSol has treaded a path of perpetual growth, expanding not only its global reach, but also the products and solutions we offer, the diverse yet detailed expertise of our team and the number of clients whose expectations we have exceeded.

Today, PharmSol has earned a worldwide reputation for developing and registering many first to file products and backward integrating. As a result, we possess a vast portfolio of products and technologies, which are either developed in-house or are co-developments. We endeavour to bring new products to the market and implement new ideas & technologies to meet needs of the future.

PharmSol is well known for offering integrated solutions with ‘single window’ access to all its clients, ensuring seamless and optimal deliverance on all assignments. In key markets and through our experience and operational flexibility, we address challenges of our customers in areas of pharmaceutical regulations, product development, registration, engineering, market affairs and supply of products.

PharmSol has widened its niche, by providing on a supplemental or comprehensive basis, fully tailored solutions for meeting the Product Development, IPR, Facility Design, Compliance, Registrations, Market Access, Audits and Supply Chain requirements, with a focus on EU, US, TGA, WHO and other International Regulatory Requirements.

PharmSol continues to strive for excellence and achieve its goal to forever be the leader in pharma and the foremost choice for its customers. Its visionary leadership, with nearly 40 years of success, continues to innovate and grow, through cementing its presence in Africa and far east Asia as well as through new ventures, such as Eminus eGlobal Institute, which are destined to transform the pharma industry.

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