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

First Class Post Graduate Degree, including the integrated PG Degrees (Computational Chemistry/Biology/ (bio) Physics/BioSciences/Chemical Biology/Bioinformatics or related areas)

Masters Degree in Biotechnology/ Agricultural Sciences/ Natural Sciences or Bachelors Degree in Engineering or Technology with specialization in Biotechnology/ Microbiology/ Molecular Biology from a recognized University or equivalent

To carry out day-to-day lab activities which includes - wet lab, cell and tissue culture, animal handling experiments, data acquiring and collating, research presentations in lab meetings and appropriate forums, actively participating in review articles, paper writing and publications.

Doctoral degree in Molecular Biology/Biochemistry/Plant Science/Life Sciences/ Biotechnology/ Bioinformatics or equivalent from a recognized university or equivalent

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.