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Officer- Formulation Development

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Onsite

Officer- Formulation Development

Rubicon Research

Officer- Formulation Development

Skills

Testing & QARInventory Management

1 month ago

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Important information


Contract type:

Permanent

Location:

Thane, Maharashtra, India

Work mode:

Onsite

Published on:

16 September 2026

What they need


IRole & responsibilities:

  • Responsible for formulation and process development of oral dosage forms, including oral solid and liquid formulations. Troubleshooting and problem-solving of unresolved or new formula issues.
  • Design and execute formulation trials and evaluate stability data to finalize formulation composition.
  • Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large scale batches.
  • Assist to alternate vendor development formulation activities along with product development of site transfer project.
  • Write/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, process validation protocols/reports, Product Development Reports, QOS etc.
  • Support the manufacturing of exhibit/submission batches per regulatory requirements.
  • Support technology transfer for manufacturing processes from laboratory scale to production scale.
  • Works with Analytical Method Development, Regulatory Affairs, Quality Control, Quality Assurance, Inventory Control, etc. to expedite the development and approval of new products by FDA.
  • Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGMPs.

Preferred candidate profile:

  • Minimum masters degree in pharmaceutical sciences with 2+ years relevant experience.
  • Candidate should have hands on/practical experience in development, technology transfer and ANDA submissions for solid/liquid oral dosage forms (solutions, suspensions, tablet, capsules) for regulated and semi-regulated markets like US, Europe and ROW.
  • Broad knowledge base of pharmaceutical sciences and processing in the Pharma industry.
  • Candidates with prior site transfer and AVD project development experience may be preferred.

Additional Notes:

  • Expected to work in any of the shifts based on the requirement.
  • Expected to visit manufacturing site whenever required.

Immediate Joiners preferable.

Interested candidates can apply or can directly share their profile on [email protected]

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