Preparation of regulatory monitor and market intelligence data. Analyse and share market intelligence data and preparation of regulatory monitor capturing key regulatory developments on monthly basis.

Preparation and submission of post approval variations and send proper communication for implementation of the change. Co-ordination with GRA, Country regulatory affiliates and COE for submission of dossier and supporting the required documentations.

Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MURA, EU with audit exposure.

Assess the performance of external manufacturing partners, identify opportunities for improvement. Ongoing performance tracking for external manufacturing, including quality, cost, delivery, and efficiency. Ensure the alignment of external sites with Teva expectations

Method Development, Method Validation, Method Verification of DS, DP as per In -House and monograph methods. Testing of analytical samples by using HPLC, GC, Dissolution, AAS, Titrations, Wet analysis.

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients. Formulation development of Pharmaceutical & Medicinal Devices

Achieve monthly, quarterly, half yearly and yearly sales target by promoting companys products ethically to customers as per the business plan, also ensure Doctor, Customer Call average as per the customer management plan of the division

After carefully observing all the instructions, the application should be submitted in the prescribed manner. Based on the information and documents provided in the application, the candidate's eligibility, ineligibility will be checked and based on that, he, she will be included in the further selection process. However, acceptance of the application or inclusion in the further selection process will not mean that the candidate is eligible for that contractual post.

Masters degree in Chemistry or Biochemistry or Pharmacy or Pharmaceutical Chemistry or Pharmacology or Bacteriology or Medicine or Microbiology or Biotechnology from a recognised university or institute.

Post graduate degree in Pharmacology or Regulatory science or a related field. Proven track record of collaborating with government bodies, academic institutions, and industry stakeholders

To undertake scientific research in the relevant areas at laboratory and in fields, including sea. PhD submitted in any branch of Science or Engineering in areas related to General Chemistry, Organic Chemistry, Pharmaceutical Chemistry. 

B Pharmacy from recognized Institute Or 10+2 with Science stream Physics Chemistry, Biology from a recognized Board. and Approved Diploma in Pharmacy from an Institute recognized by the Pharmacy Council of India and registered as Pharmacist under the Pharmacy Act 1948.

Masters degree, diploma, life sciences, pharmacy, public health, healthcare or other related discipline with minimum 2 years of relevant clinical trial monitoring experience.

To carry out day-to-day wet-lab research activities in the lab of Dr Reena Singh – Cardio Met Translational lab. Self-driven candidates interested in Developmental and Stem Cell Biology with experience in immunocytochemistry, imaging, Molecular Biology, Cell, Tissue culture, and FACS experiences are preferred but are not mandatory requirements for the application.

ECHS invites applications to engage following Medical, Para Medical & Non Medical Staff on contractual basis in ECHS Polyclinic Shillong for a period of one year (w.e.f 01 Apr 2025) renewable for additional period of one year / till attaining the maximum age subject to performance of candidates / other conditions according to the criteria as mentioned against each post.

Thalidomide as treatment of basal exudates in Tuberculous Meningitis : A prospective randomized open blinded endpoint PROBE study. Post Graduate Degree in Basic Science OR Graduate, Post Graduate Degree in Professional Course selected through a process described through National Eligibility Tests - CSIR-UGC NET including lectureship Assistant Professorship and GATE.

Responsible for processing of Individual Case Safety Reports ICSRs from various sources, Literature search and review, signal detection and management, tracking regulatory information, performing regulatory submissions and supporting preparation of aggregate and other study reports, as well as Medical and Product Dictionary Management activities, where applicable 

Manufacturing process like Autoclave, vial washing, filling ,Coating, compression ,capsule filling and packing. Microfluidizer equipment handled ,CIP,SIP system, Lyophilizer

Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA.