Freshers Needed In Executive – Regulatory Affairs / Research Associate – Analytical At Piramal Pharma

Piramal Critical Care, a business unit of Piramal Pharma, has announced openings for Executive – Regulatory Affairs in Mumbai and Research Associate – Analytical in Rabale, Maharashtra. The positions are in Regulatory Affairs and R&D Analytical Development, respectively.

Eligible candidates with relevant pharmaceutical or scientific qualifications can review the job responsibilities, experience requirements and application links below.

Piramal Pharma Job Details

1. Executive – Regulatory Affairs

Job Location: Kurla, Mumbai, Maharashtra
Department: Regulatory Affairs
Experience: 2–4 years
Qualification: M.Pharm, B.Pharm, M.Sc. or equivalent in a relevant scientific discipline
Travel Requirement: Low

Job Description

The Executive – Regulatory Affairs will support regulatory submissions, including new marketing authorisations, variations and renewals, for European and Rest of World (RoW) markets. The role focuses on ensuring compliance with applicable legislation, regulatory guidelines and national requirements to support product supply.

Roles and Responsibilities

• Prepare and submit regulatory documentation for new marketing authorisations, variations and renewals.
• Prepare and review regulatory applications, dossier components, SmPCs and product labelling.
• Ensure submissions comply with applicable regulations, local procedures and guidelines.
• Initiate change controls for regulatory-driven changes.
• Coordinate with project teams to collect submission-related information.
• Prepare and review responses to Requests for Information (RFIs) from Health Authorities.
• Coordinate artwork and labelling updates, including serialization projects, marketing authorisation transfers and variations.
• Manage requests for complementary documents, including Certificates of Pharmaceutical Product (CPPs) and declarations.
• Maintain regulatory documentation, databases, activity trackers and electronic filing systems.
• Collaborate with internal departments and external stakeholders to meet project timelines.
• Contribute to process improvements and prepare or revise SOPs and work instructions.
• Monitor regulatory changes and communicate updates to relevant teams.
• Support regulatory submission strategies for new applications and complex variations.

Eligibility and Required Skills

Candidates should have:

• M.Pharm, B.Pharm, M.Sc. or an equivalent qualification in a relevant scientific discipline.
• 2–4 years of relevant experience handling European markets and/or Rest of World territories.
• Strong written and spoken English communication skills.
• Proficiency in Microsoft Word and Excel.
• Attention to detail and the ability to critically review regulatory documents and data.
• Strong coordination and collaboration skills for working with global teams.
• The ability to manage multiple projects, prioritise tasks and meet deadlines.
• Good technical knowledge of pharmaceutical or allied industries.
• Knowledge of regulatory requirements and the ability to track changes in applicable guidelines.

Apply for Executive – Regulatory Affairs

Last Date to Apply: November 18, 2026

2. Research Associate – Analytical

Job Location: Rabale, Maharashtra
Department: R&D Analytical Development
Qualification: M.Sc. in Chemistry or a related discipline
Experience: 0–4 years

Job Description

The Research Associate – Analytical will support R&D Analytical Development projects involving APIs, formulations, speciality chemicals and analytical testing methods. The role includes analytical method development, validation, method transfer, laboratory management and compliance with cGMP and CGLP requirements.

Roles and Responsibilities

• Perform scientific research activities using established techniques, procedures and laboratory equipment.
• Support experimental planning and investigate technical concepts and requirements.
• Develop and validate analytical methods for APIs, formulations, raw materials and excipients under managerial supervision.
• Use analytical instruments such as HPLC, GC, IR and auto titrators.
• Support analytical method transfer to manufacturing sites and troubleshoot technical issues.
• Generate, interpret and review analytical data for APIs and formulations.
• Analyse development batches and routine stability samples.
• Prepare standard test procedures, SOPs and IOPs.
• Support plant, Regulatory Affairs and Quality Assurance teams in resolving analytical queries.
• Maintain laboratory equipment, reagent and column inventories, calibration records and IQ/OQ/PQ documentation.
• Follow cGMP and CGLP requirements and implement laboratory SOPs.
• Prepare analytical method transfer documentation, including assessment documents, transfer plans, protocols, reports and stability data.
• Coordinate with team members and support on-site or off-site technology transfer activities.

Eligibility and Required Skills

Candidates should have:

• An M.Sc. in Chemistry or a related discipline.
• 0–4 years of experience.
• Strong knowledge of analytical chemistry and industrial analytical techniques.
• Experience using HPLC, GC, IR, auto titrators and other sophisticated analytical instruments.
• A basic understanding of analytical method development, validation and transfer.
• Knowledge of Quality Management Systems (QMS), ICH guidelines and cGMP.
• The ability to interpret analytical data, draw conclusions and present results.
• Technical writing skills.
• Proficiency in Microsoft Word, Excel and PowerPoint