Here is the rewritten content, adhering to your specified requirements:
Aresko Life Sciences: Driving Innovation in Pharmaceutical Manufacturing
Aresko Life Sciences stands as a rapidly growing force in the pharmaceutical industry, specializing in the advanced development and manufacturing of Active Pharmaceutical Ingredients (APIs), crucial intermediates, and a range of hormone products. The company prides itself on operating modern manufacturing facilities that rigorously comply with leading international regulatory bodies, including the USFDA, MHRA, and TGA. This commitment to global standards ensures the delivery of high-quality pharmaceutical products to markets worldwide. Aresko Life Sciences is dedicated to fostering a culture of excellence and offers outstanding career opportunities for seasoned professionals across critical areas such as Research & Development, Engineering, Production, Quality Control, Quality Assurance, and Regulatory Affairs.
Exclusive Walk-In Interview Event
Experienced pharmaceutical professionals are invited to a special walk-in interview drive on Sunday, July 5th, 2026. This event provides a unique chance to join a forward-thinking organization that values expertise and dedication. Interviews will be conducted from 9:30 AM to 5:30 PM at Hotel Ginger Bharuch, Sethna Plaza Annexe, Station Road, Bharuch, Gujarat – 392001. Please note that the primary work location for all selected candidates will be at the company’s state-of-the-art facility in Kashipur, Uttarakhand.
Career Opportunities for Experienced Professionals:
Aresko Life Sciences is actively seeking candidates with 2 to 12 years of experience in the pharmaceutical or API manufacturing sector, particularly those with a background in USFDA, MHRA, or TGA regulated environments.
-
Research & Development (R&D):
- Research Scientist (M.Sc, 8-12 Years): Specializing in API process development, route scouting, organic synthesis, process optimization, scale-up, technology transfer, GMP compliance, impurity profiling, and regulatory documentation (DMF/ANDA).
- Research Associate / Chemist (M.Sc, 3-8 Years): Focused on organic synthesis, laboratory experimentation, API process development, reaction optimization, GMP awareness, and technology transfer support.
-
Engineering:
- Manager / Deputy Manager / Assistant Manager (B.Tech Mechanical, 8-12 Years): Expertise in engineering maintenance, utilities management, preventive & predictive maintenance, reliability engineering, validation, calibration, CAPEX management, and GMP compliance.
- Executive / Senior Executive (B.Tech Electrical, 5-10 Years): Proficient in electrical maintenance, LT/HT systems, DG & UPS, MCC, switchgear, PLC/VFD troubleshooting, HVAC, energy management, and EHS compliance.
-
Production (Any Graduate / B.Com / M.Com, 2-10 Years):
- Openings for Operator, Chemist, Officer, and Senior Executive roles. Key skills include API production, reactor & centrifuge operations, filtration, drying, material charging, strict adherence to GMP, SOPs, BMR documentation, QMS, CAPA, and regulatory compliance.
-
Quality Control (B.E./B.Tech/M.E./M.Tech Mechanical/Electrical/Civil Engineering – as per original details, 2-7 Years):
- Officer, Senior Officer, Executive, and Senior Executive positions. Requires strong knowledge of GMP, GLP, analytical techniques (HPLC, GC, wet chemistry), reviewer roles, microbiology, laboratory investigations (OOS/OOT/OOE), stability studies, and documentation.
-
Quality Assurance (B.Pharm / M.Pharm / B.Sc / M.Sc, 2-10 Years):
- Officer, Senior Officer, Executive, and Senior Executive roles. Responsibilities include QMS, investigations, documentation review, OOS/OOT, deviations, CAPA, change control, market complaints, IPQA, analytical QA, validation, and batch release.
-
Regulatory Affairs (Executive) (M.Sc / M.Pharm, 5-8 Years):
- Key skills involve CTD compilation, DMF preparation, R&D/QC/QA data compilation, GMP compliance, ICH guidelines (Q7/Q8/Q9/Q11), data integrity, regulatory submissions, and cross-functional coordination.
General Eligibility Criteria:
Candidates should possess relevant experience ranging from 2 to 12 years, depending on the specific role. Required qualifications include Any Graduate, B.Com, M.Com, B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, or M.Tech. Mandatory prior exposure to USFDA, MHRA, or TGA regulated manufacturing environments is essential, preferably within the API, Intermediate, or Hormone manufacturing sectors.
Documents Required for Interview:
All attending candidates must bring an updated Resume/CV, Aadhaar Card, the last three months’ salary slips, all educational certificates, experience certificates, and passport-size photographs.
Contact Information:
For any preliminary queries regarding these opportunities, candidates may contact the company directly at gs@aresko.com.
Why Join Aresko Life Sciences?
Aresko Life Sciences offers a dynamic and rewarding career path within a globally compliant manufacturing environment. Professionals will gain invaluable exposure to cutting-edge API and hormone manufacturing processes and advanced technologies. The company provides diverse career opportunities across its R&D, Engineering, Production, Quality Control, Quality Assurance, and Regulatory Affairs departments. Joining this team means becoming part of a collaborative environment that prioritizes innovation, stringent compliance, and continuous professional growth, offering excellent learning experiences with international regulatory standards.
