Pharma Jobs in Maharashtra: Teva is Hiring a Formulation Researcher I | Apply Now for Teva Career
If you are currently looking for Pharma Jobs in Maharashtra, here is an opportunity. Teva Pharmaceuticals, a global leader in generic and specialty medicines, is looking for a Formulation Researcher I to join its team in Ambernath, India. This role offers the opportunity to contribute to the development of high-quality, affordable medicines that impact millions worldwide. Ideal candidates will bring strong analytical acumen, experience in formulation research and development, and the ability to collaborate across global teams to deliver excellence from product conception to launch. Apply now for this pharma job and kickstart your career with Teva career.
Job Details:
- Job Title: Formulation Researcher I
- Location: Ambernath, India, 421506
- Job Id: 64724
About the Company:
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to improving the health and quality of life for millions of people around the world. With a legacy spanning over 120 years, Teva combines innovation, science, and accessibility to deliver high-quality, affordable treatments across major therapeutic areas such as neurology, oncology, respiratory care, and pain management.
Operating in nearly 60 countries, Teva is recognized as one of the world’s largest producers of generic medicines, serving over 200 million patients daily. The company’s commitment to research and development, regulatory excellence, and sustainability ensures continuous advancement in global healthcare. At Teva Career, every employee contributes to a shared mission — making good health more affordable and accessible for all.
Education and Experience:
Ph.D. in Pharmaceutical Sciences with 1 Yrs +/ M.Pharm in Pharmaceutical Sciences with 3yrs+ from reputed universities. Experience in working in high performance teams in known generic space/organizations with known generic footprint in regulated markets. Viz. US/EU/Canada.
Key Responsibilities:
- Work on bench with the formulation development teams for the timely achievement of key milestones.
- Planning and conducting of experimentation in line with QbD paradigm, using OFATs and DOE.
- Preparing Presentations during Products development at all stages (Day 0, Development stage, Pilot BE, Scale-up, EB Phase gate, Filling and Launch Phase gate) and discuss/interpret the data.
- Conduct literature review, prior art experiment design of the product identified for development.
- Evaluate API & Excipients sources and Innovator product identification, procurement, characterization and reverse engineering.
- Conduct and interpret data from Preformulation studies viz. Compatibility studies, API particle size finalization (malvern/SEM/Raman), API Solubility studies, polymorphic form-phase transformation studies, selection of excipients and process as per strategy.
- Conducting and performing the development trial at bench level, problem identification & resolution.
- Review and interpretation of analytical data for further action plan.
- Responsible for execution of Pilot BE batches and interpretation of bio results.
- Responsible for execution of scale-up and exhibit batches at different manufacturing location with coordination of cross functional team and interpretation of Pivotal bio results.
- Identify Quality Target Product Profile (QTPP), Critical Quality Attributes (CQAs), Critical Process Attributes (CPAs) and subsequent use of Design of experimentation (DOE).
- Establish the stability data for development batches in collaboration with the analytical team.
- Master document preparation like MFC, Scale up batch study protocol/report, sampling plan, stability guidance documents, In-use stability study protocol/report.
- Coordination with various CFT’S like sourcing, Project Management, analytical, Regulatory, Packing, Production, MSAT, DQA and clinical for smooth development of product.
- Compilation and preparation of pharmaceutical development report with respect to current QbD format.
- Responsible for preparation of Product Developmental Report (PDR) for filling.
- Handling of deviations, change control and OOS related to Exhibit batches.
- Preparation, updation of SOPs.
- Maintaining of batch, calibration and other necessary records.
- Subjecting required batches to stability studies.
Knowledge and Skill required:
Technical skills
- Formulation Development of Solid Oral Dosage forms, exposure from development and submission to regulatory agencies.
- Uses established process, scientific theories and principles to solve problems.
- Good learning acumen.
- Basic level understanding on recent ICH, regulatory guidelines, IP requirements; understanding of Bioequivalence, GMP, Quality and SOP compliance, GLP etc.
People Skills
- Must be confident, able to work in the team and a good team player.
- Stable and calm, Supports functional colleagues.
- Has the ability to take comprehend facts and data to help the decision making.
- Shows respect, listens effectively, shows caring & be compliant with the core values of TEVA.
- Demonstrates timeliness.
Interpersonal Skills
- Collaborates with team within functional area and cross functional teams.
- Good technical communication applied locally and contributor to local and/or global project teams.
- Delivers technical presentations.
- Ability to work with very little supervision, work with junior staff.
- Ability to work independently on individual products.
- Ability to work with internal and external partners.
