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Pontika Aerotech Limited, a USFDA-approved state-of-the-art contract research and manufacturing organization based in Paonta Sahib, Himachal Pradesh, is hiring for Quality Control (Chemist/Officer/Sr. Officer) roles.
Established in 2017, Pontika excels in pharmaceuticals, Ayurveda, and cosmetics, delivering innovative solutions across diverse segments like topical pharmaceuticals, personal care, and hygiene products.
With cutting-edge technology and a quality-centric culture, we are one of India’s fastest-growing CDMOs. Join our team to drive excellence in pharmaceutical quality control!
Note: Candidates must have experience in pharmaceutical formulations (preferably aerosols, topicals, or OSD). API-only experience may not be sufficient. Pontika Aerotech does not charge any fees for job applications. Beware of fraudulent invitations requesting payment; contact careers@pontikaaerotech.com for verification.
Job Details
- Department: Quality Control (QC)
- Designation: Chemist / Officer / Sr. Officer
- Location: Pontika Aerotech Limited, Vill. Johron, P.O. Puruwala, Nahan Road, Paonta Sahib, Dist. Sirmour, Himachal Pradesh – 173001
- Qualification: B.Pharm / M.Sc. (Chemistry, Analytical Chemistry, or related fields) / B.Sc.
- Experience: 1-5 Years in pharmaceutical quality control (experience in aerosols, topicals, or OSD formulations preferred)
Key Responsibilities:
- Perform analysis of raw materials, packing materials, in-process samples, and finished products (e.g., aerosols, creams, tablets).
- Conduct chromatographic analysis using HPLC and GC with proficiency in software like Empower or Chromeleon.
- Operate and maintain analytical instruments (e.g., UV, FTIR, dissolution apparatus, KF titrator) and perform calibrations/preventive maintenance.
- Execute analytical method validation, method transfer, and stability studies per ICH guidelines.
- Manage stability chamber operations and analyze stability samples.
- Review QMS documents (e.g., SOPs, STPs, specifications, validation protocols).
- Support regulatory audits (e.g., USFDA, WHO) and handle OOS, OOT, deviations, and CAPA documentation.
- Ensure compliance with cGMP, USFDA (21 CFR Part 210, 211), and ICH guidelines.
Key Skills:
- Hands-on experience with HPLC, GC, and other analytical instruments.
- Strong knowledge of analytical method validation, method transfer, and stability studies.
- Familiarity with GLP, GMP, and regulatory compliance for formulations.
- Problem-solving skills and attention to detail in documentation.
Why Join Pontika Aerotech?
- Industry Leader: Work with a USFDA-approved CDMO with a focus on innovative aerosols, topicals, and cosmetics, generating USD 20 million annually [Web:17].
- Innovative Environment: Contribute to cutting-edge R&D and manufacturing in a facility rated 3.8/5 for salary and benefits [Web:10].
- Career Growth: Access training and career advancement in a dynamic, entrepreneurial culture fostering innovation [Web:8].
- Benefits: Competitive salary (average ₹3-7.2 Lakhs for QC roles [Web:19]), health insurance, and a supportive work environment.
Learn more about our mission at Pontika Aerotech and industry standards at USFDA or ICH.
How to Apply
- Email Application: Send your updated CV to careers@pontikaaerotech.com. Mention “Quality Control [Designation] Application” (e.g., “Quality Control Officer”) in the subject line.
- Contact: For queries, call +91 9805514664.
- Requirements: Include CV, educational certificates, last 3 months’ salary slips (if applicable), and a cover letter highlighting your QC experience in formulations.
- Stay Updated: Follow #PharmaJobs and #PaontaSahibJobs on X.com for the latest pharmaceutical career opportunities.
Join Pontika Aerotech to drive quality and innovation in pharmaceutical manufacturing!