Company Description SEQENS is a global leader in pharmaceutical solutions and specialty ingredients, serving customers across Europe, North America, and Asia. The group operates 15 manufacturing sites and 5 R&D; centers, supported by 2,700 employees, including 300 scientists, engineers, and technical experts. As an integrated player, SEQENS offers a broad portfolio of active ingredients, pharmaceutical intermediates, and specialty ingredients.

The company focuses on developing and industrializing complex, high-value molecules and invests in advanced technologies to deliver innovative, tailored solutions for customers. Team members join a collaborative environment dedicated to scientific excellence and continuous improvement.

Role Description The Manager Analytical Method Validation is a full-time, on-site role based in the Pune Division. This role is responsible for planning, executing, and overseeing analytical method validation activities to ensure compliance with regulatory and internal quality standards. Daily tasks include designing validation protocols, reviewing and interpreting analytical data, preparing technical reports, and coordinating with Quality Assurance, Quality Control, and production teams.

The manager leads and mentors laboratory staff, ensures proper use and maintenance of analytical instruments,



and supports troubleshooting of methods and equipment. The role also involves participating in audits, implementing best practices in laboratory operations, and driving continuous improvement in analytical methodologies and documentation.

Qualifications

- Candidates should possess strong Supervisory Skills, including team leadership, mentoring, and performance management.
- Candidates should possess robust Quality Control and Quality Assurance skills to maintain compliance with GMP and regulatory guidelines.
- Candidates should possess advanced Laboratory Skills and practical experience with analytical techniques and instrumentation.
- Candidates should possess solid Chemistry knowledge, preferably in analytical or pharmaceutical chemistry.
- Relevant qualifications such as a bachelor’s or master’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
- Experience in analytical method development and validation within the pharmaceutical or chemical manufacturing industry.
- Strong documentation, data analysis, and report-writing skills, with attention to detail and accuracy.
- Ability to collaborate cross-functionally, manage multiple projects, and meet timelines in a regulated setting.

📌 Manager Analytical Method validation (Pune)
🏢 Seqens
📍 Pune