Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Hetero group employs over 21,000 people. Hetero is a player in the active pharmaceutical ingredients market and finished dosages. It has marketing presence in over 127 countries. Hetero has supplied antiretroviral drugs to patients across more than 100 countries globally.
🌟 Walk-in Interview for QA & QC Professionals at Hetero Drugs Ltd. 🌟 Excellent opportunity for B. Pharmacy & M.Sc. Chemistry with QA & QC Experienced Candidates.
We are seeking talented candidates to join HETERO LABS & DRUGS LIMITED in Nakkapalli, Anakapalli, Andhra Pradesh. If you have relevant experience and are looking for new opportunities, we invite you to apply for the following current openings:Â Â
Positions Available:
Quality Control (API) – 06 to 10 years of experience
-
We are seeking individuals with practical expertise in API operations QMS, AQA, Validation, Dispatch, and Candidates should hold a degree in B.Pharmacy or M.Sc.
Quality Assurance( API) – 03 to 08 Years of experience
- We are seeking particularly skilled in handling GC, HPLC, and Wet Lab, and Candidates should hold a degree in B.Pharmacy or M.Sc.
Walk-In Interview Details:
- Date: 27th July 2024
- Venue: Neha Vilas Bhavan, Kurmanpalem, Vizag.
- Work Location: Hetero Drugs, Nakkapalli
-
Mail ID: Anil.l@hetero.com
Registration Link: Click Here
We are seeking talented candidates to join HETERO LABS & DRUGS LIMITED in Nakkapalli, Anakapalli, Andhra Pradesh. If you have relevant experience and are looking for new opportunities, we invite you to apply for the following current openings:Â Â
Are you an expert in Quality Assurance with a strong background in Quality Management Systems (QMS), Validations, Dispatch, Review, and Change Controls? We have an exciting opportunity for you!
Job Description:
As a Quality Assurance Specialist at Hetero, you will play a pivotal role in ensuring our products meet rigorous quality standards. Your responsibilities will include:
- Implementing and maintaining Quality Management Systems (QMS) to ensure compliance with regulatory requirements.
- Conducting validations and verifications of processes, equipment, and systems to uphold quality standards.
- Overseeing dispatch processes to ensure timely and accurate delivery of products.
- Reviewing documentation and procedures to identify areas for improvement and compliance.
- Managing Change Controls to maintain product quality throughout lifecycle changes.
Requirements:
- B. Pharmacy or M.Sc. in a relevant field (e.g., Quality Assurance).
- Proven experience in Quality Assurance with a focus on QMS, Validations, Dispatch, Review, and Change Controls.
- Strong knowledge of regulatory requirements (e.g., GMP,FDA, ISO) and quality standards.
- Excellent attention to detail and analytical skills.
- Effective communication and collaboration skills to work across teams and levels.
-
- Performing analytical testing using techniques such as HPLC and GC to assess the quality of raw materials, packaging materials, and intermediates of API products.
- Developing and reviewing specifications and Standard Testing Procedures (STP) for RM, PM, and Intermediates to ensure accuracy and compliance.
- Ensuring effective maintenance, cleaning, and calibration of analytical instruments (HPLC, GC) to maintain reliability and accuracy of results.
- Collaborating with cross-functional teams to resolve analytical issues and support continuous improvement initiatives.
- Contributing to regulatory submissions and inspections by providing accurate analytical data and documentation.Job Description:
You will be responsible for ensuring the quality and compliance of our products through meticulous analysis and adherence to regulatory standards. Your key responsibilities will include:
- Requirements:
- M.Sc. in Organic Chemistry or Analytical Chemistry.
- 3 to 15 years of experience in a pharmaceutical or related industry.
- Strong proficiency in analytical techniques such as HPLC, GC, and knowledge of spectroscopic methods.
- Experience in preparing and reviewing specifications and STPs for RM, PM, and Intermediates of API products.
- Proven ability to ensure effective maintenance, cleaning, and calibration of analytical instruments.
- Knowledge of regulatory requirements (e.g., FDA, ICH guidelines) related to analytical testing and documentation.
Like what you’re seeing and if you found the write up useful, would love to hear your feedback in the comment section. Do share, like and follow for more on Facebook, Instagram, Twitter, Telegram, Whatapp & Whatapp Channel.
Related Jobs: Dr.Reddy’s Biologics – Opportunity Exclusively for Women in Quality Control / Quality Assurance / Drug Substance Departments
Follow the Pharma Wisdom Jobs channel on WhatsApp: Click Here
More Job Updates Join What’s App Group – Click Here
Join Telegram Group – Click Here
