Strong knowledge of GMP regulations including WHO, EU GMP, PICS, TGA, MHRA, USFDA & other global regulatory guidlines. Expertise in handling CAPA, CCF, deviations, market complaints, product recalls if any.

Good Academic record with First Class Masters Degree in Chemistry/Biochemistry/Biotechnology with a qualified National Eligibility Test–CSIR-UGC-NET/LS or DBT-BET/ ICMR/Fellowship or GATE

Preparation & review of New and Existing Products artwork. Responsible to maintained artworks track records in excel.

Preparation and Execution of qualification protocols for Equipment's, Autoclave, Tunnel, Filling and capping machine, Lyophilizer, Washing machine, bung processor etc.

Macleods is one of the fastest growing pharmaceutical company, having strong presence in various therapeutics segments. Ranked amongst the top 10 companies.

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India

To perform the role & responsibilities defined as per TMS software. Escalation to Superior for major non- conformities timely.

Skilled in medical device packaging and Visual inspection, with expertise in strategic planning, documentation, aligned with cGMP standards.

Assist in the preparation of response packages to Health Canada requests in a timely manner to minimize delays in the submission review process. 

Designs and coordinates the overall direction of clinical development projects. Coordinates activities of associates and investigators to ensure compliance with protocol and overall pre-clinical objectives. Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings

Bachelors degree in life sciences, pharmacy, or a related field. An advanced degree is preferred. Extensive experience in pharmacovigilance or drug safety reporting, with a strong understanding of relevant regulations and guidelines.

B. Pharmacy/D.Pharmacy/ Pharma-D/M.Pharmacy course after intermediate recognized by the Govt, of A.P.  Any other eligible equivalent Qualification must be registered With AP Pharmacy council with Updated renewal. 

B.Pharm / M.Pharm ; Preference will be given to candidates who have experience working in clinical trials.

B.Pharma or Bachelors degree in Engineering or Technology or Medicine or from a recognized University of equivalent. 

Ph.D in Bioengineering, Biomedical engineering, Mechanical Engineering with First class or equivalent grade at the preceding degree M.Sc, M.Pharm, M.S.Pharm, B.Tech, M. Tech in relevant field with a very good academic record.

Liaison Officer will maintain database of all projects, update project changes, act as link between the SRC and the project personnel to facilitate smooth function of ISRC-I & II, NIEC l & ll meetings.

First Class Post Graduate Degree in relevant subjects Public Health, Life Sciences, Biostatistics, Epidemiology, Biotechnology.

Applicants having postgraduate degree and holding a valid Junior Research Fellowship from CSIR, UGC, DBT, ICMR, BINC can apply.

Post Graduate Degree in Life Sciences/ Post Graduate degree in the professional course selected through a process described through National Eligibility Test- CSIR-UGC NET including lectureship and GATE.