Home / Job / Jiaan Biotec – Walk-In Drive for QC Chemist / Quality Analyst on 20th & 21st Oct’ 2020

Jiaan Biotec – Walk-In Drive for QC Chemist / Quality Analyst on 20th & 21st Oct’ 2020

Jiaan Biotec – Walk-In Drive for QC Chemist / Quality Analyst on 20th & 21st Oct’ 2020

Opening for QC Chemist and Quality Analyst (Executive/ Asst Manager)

Roles and Responsibilities:

  1. Assist in QC stability testing, prepare and maintain stability records and summaries.

  2. Modify and validate analytical procedures to meet QCs needs.

  3. Support design and development of experimental protocols, SOPs, etc., consistent with cGMP/GLP.

  4. Participate in special projects and department meetings via input, feedback and execution of assigned tasks.

  5. Execute special projects on analytical and instrument problem solving.

  6. Conduct all quality QC chemical tests.

  7. Perform non-radioactive and biological QC on time and record quality of product.

  8. Adapt, maintain and operate analytical instrumentation.

  9. Involve in procedure review and propose modifications and updates.

  10. Ensure work environment is clean and safe complying with safety and pharmaceutical regulation.

  11. Conduct radiation safety duties conforming to regulations.

  12. Report monthly on supplies for QC orders involving devices and reagents.

  13. Contribute to industrial, R&D qualification and validation activities and support routine maintenance.

  14. Conduct various analytical testing procedures as per manufacturing/QC SOPs.

Desired Candidate Profile:
1. Documenting/Recording Information Entering, transcribing, recording, storing, or maintaining information in written or on computer.

  1. Interacting With Computers Using computers and computer systems (including hardware and software) to program, write software, set up functions, enter data, or process information

  2. Communicating with Supervisors, Peers, or Subordinates Providing information to supervisors, co-workers, and subordinates by telephone, in written form, e-mail, or in person.

  3. Analyzing Data or Information Identifying the underlying principles, reasons, or facts of information by breaking down information or data into separate parts.

  4. Processing Information Compiling, coding, categorizing, calculating, tabulating, auditing, or verifying information or data.

  5. Identifying Objects, Actions, and Events Identifying information by categorizing, estimating, recognizing differences or similarities, and detecting changes in circumstances or events.

  6. Evaluating Information to Determine Compliance with Standards Using relevant information and individual judgment to determine whether events or processes comply with laws, regulations, or standards.

Date: 19th October – 21st October, 10.00 AM – 5.30 PM

Venue:

303-304, krishna tower, opps curewell hospital,

Near zanjeerwala circle,

Indore

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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