Leading, fully integrated pharmaceutical formulation development, manufacturing, and marketing company Intas operates internationally. Through a comprehensive pharmaceutical value chain that spans the globe, Intas is dedicated to addressing unmet medical and societal needs. To operate in international markets, Intas has established a network of companies under the banner name of Accord Healthcare. Intas has evolved over the years both organically and through acquisitions, increasing its operations and product line year after year. With a strong sales, marketing, and distribution infrastructure in regions like North America, Europe, Central & Latin America, Asia-Pacific, CIS, and MENA countries, it is currently active in more than 85 countries globally.
Designation: Officer – Senior Officer
Department: Quality Control & Microbiology
Qualification: M.Sc. / B.Sc.
Experience: 2 to 5 years (Having experience of instruments like HPLC, GC, UV, IR)
Designation: Executive – Senior Executive
Department: QA – Microbiology
Qualification: M.Sc. (Micro.)
Experience: 5 to 8 years (Technical expert for all micro related questions, issues and decisions in the organization including aseptic techniques and procedures.)
Designation: Executive – Senior Executive
Department: Data Integrity (Formulation & API)
Qualification: M.Sc. / B.Pharm / M.Pharm
Experience: 4 to 8 years (All possible Data Integrity, EBMR, Document, Logbooks, Handling of paper, Audit Trail vs actual execution at site.)
Designation: Officer – Senior Officer
Department: Solid Oral (Tablet Manufacturing)
Qualification: B.Pharm
Experience: 2 to 6 years (Having Experience in Granulation / Compression / Coating / Inspection.)
Designation: Officer – Senior Officer
Department: Oncology Parenteral
Qualification: B.Pharm / M.Pharm
Experience: 2 to 5 years (Exposure to work in Bulk Manufacturing / Mfg skid with multiple vessel / NDDS area, Aseptic filling SVP, Lyophilization, Media fill, Qualification, QMS.)
Designation: Senior Officer – Executive
Department: QA – Validation & Qualification (OSD & injectable)
Qualification: M.Sc. / B.Pharm / M.Pharm
Experience: 4 to 8 years
Desirable:
Process and Cleaning validation, protocol report and risk assessment.
Equipment qualification documents (URS, FAT, SAT, DQ, IQ, OQ, PQ) & Compliance mgt.
SME in HVAC validation, Equipment Qualification
Designation: Associate
Department: Oncology Parenteral
Qualification: ITI / Diploma
Experience: 2 to 5 years
Can operate Manufacturing skid with multiple vessel, Worked in Aseptic area SVP line, can operate Filling machine / cRABS / Isolator with 21CFR compliance, Autoclave, Vial washing and depyrogenation tunnel.
Exposure to regulatory audit.
Walk-in Interview Date: 16 April 2023 (Sunday)
Time: 10:00 am to 05:00 pm
Venue: The Fern Kesarval Hotel, Bus Stand, Kesarval Gardens, Edapally – Panvel Hwy, Quelossim, Goa.
