SP ACCURE LAB-INTERVIEWS on 24 Feb 2024

SP ACCURE LAB-INTERVIEWS on 24 Feb 2024

SP ACCURE LAB-INTERVIEWS on 24 Feb 2024
Department
Regulatory Affairs (EU/AUS)Need for Europe/Australia Region (Review, compilation of docciers, RFIs, Variations) End to End Activities/Jr. Executive /Executive/ Sr. Executive/M.Pharm, B.Pharm, MSc and UG/2-8 Yrs
Regulatory Affairs RoW/WHOReview, compilation of Dossiers for RoW Region (Asea, Africa, Latam, GCC) in CTD/ACTD/Country specific formats, Renewals, Tenders, Variation/Jr. Executive /Executive/ Sr. Executive/M.Pharm, B.Pharm, MSc and UG/2-8 Yrs

Quality Control
GLP Activities-2 no’s/Jr. Executive/Executive/M.Pharm, B.Pharm, MSc (Chemistry)/3-7 Yrs
Quality Control
Raw material and GC Operations-3 no’s/Jr. Executive/Executive
M.Pharm, B.Pharm, MSc (Chemistry)/2-5 Yrs
Warehouse
Raw materials and packing materials -1 Handing of FG-1Boc,/Handing of receipts and Documents -1/Jr. Executive/B.Com Bsc/4-5 Yrs
DATE: 24.02.2024 (Saturday) Time: 10:00 AM to 04.00 PM

Candidates who are unable to attend the interview can mail your updated resumes to [email protected] Should have relevant experience for above said positions.
DOCUMENTS REQUIRED:
1. Updated Resume
2. Recent Increment Letter/Offer Letter with CTC Break up
3. Latest 3 months Payslips
4. Copy of all Educational Certificates
5. Copy of Aadhar
INTERVIEW VENUE:
SP Accure Labs Pvt.Ltd.,
Plot No.12, Biotech Park Phase-II, Lalgadi Malakpet (V), Shamirpet (Mandal), Medchal-Malkajgiri, Telangana- (500101), INDIA.

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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