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Gland Pharma (March-2020)

Gland Pharma Ltd.Walk in Interview On 17th Mar For Microbiology only Male Candidates are Eligible
  • Post Name: Microbiologist
  • Qualification: B.Sc in Bio-Chemistry, Microbiology,
  • MS/M.Sc(Science) in Bio-Chemistry, Biotechnology, Microbiology
  • Experience :1 – 4 years
Documents Required :

 

  • Passport size Photograph 4 Nos.
  • Your updated resume
  • Photocopies of Qualification certificates
  • Photocopies of Aadhar Card/Pancard
  • Experience/Service certificates
  • Salary certificate / latest three months pay slip from the present employer with supporting bank statement/ CTC Structure.

mportant details:

  1. Location: Hyderabad
  2. Salary : NA
  3. Openings : 05

Time and Venue :17th March , 9 AM onwards contact Person: Ms Latha- Gland Pharma Ltd. TSIIC-IP, III Phase, Plot No: 42 to 52 Pashamylaram, Patancheru, Sangareddy District. Pin: 502307. Land Mark: Besides KIRBY Lane.Phone Number 08455222000 Contact – P.Latha(223635)

Aurobindo Pharma (March-2020)

Aurobindo Pharma. Walk in For Regulatory Affairs Department – Formulation (Ongoing 17 March 2020)

  • Job description

    We are looking for candidates who are having relevant experience in Formulation Regulatory Affairs.

    Department: Regulatory Affairs – Europe/ US/ Canada/ South Africa Market only
    Qualification: B.Pharm/ M.Pharm
    Experience: 2-14 Years of experience
    Skill Required: Labeling/ CMC/ Life Cycle Management
    Location: Hyderabad
  • Detailed JD:
    1. Competent with Europe/ US/ Canada/ South Africa -filing requirements with respect to Modules 2 & 3. Ability to independently and effectively review technical documents related to
    2. Well versed with Europe/ US/ Canada/ South Africa -Regulatory Guidance and Processes (i.e. Ability to understand and interpret technical expectations as per applicable ICH and Europe/ US/ Canada/ South Africa guidelines)
    3. Sound knowledge of basic aspects of a Formulation (primarily pharmaceutical development along with general analytical aspects)
    4. Should be aware of Post-approval variation requirements in Europe/ US/ Canada/ South Africa and have ability to take decisions related to the variation categorization. Should have basic QA knowledge to enable correct review of related change controls and decide on any impact on regulatory front in terms of variation.
    Full Time, Permanent
    R&D
    Education
  • B.Pharma in Pharmacy
    M.Pharma in Pharmac
 
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