QC Associate

Found in: Whatjobs IN C2 - 2 weeks ago


india PSC Biotech Ltd Full time
Job Description
About PSC Biotech
Who we are?
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

Description: 24/7 Shift Roles @ 35% shift premium.


Requirements

Responsibilities include but are not limited to:

 

·        Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.

·        Review and authorisation of Lab Data

·        Support Analytical Technical Transfer activity testing reports and documentation.

·        Document review/updates when required.

·        Equipment Calibration, Maintenance and Trouble Shooting.

·        Method Validation/Verification.

·        Training of QC Chemistry Laboratory colleagues.

·        Laboratory Investigation support

·        Laboratory Housekeeping and maintaining GMP standards.

·        Assisting in regulatory audits.

 

 

The successful candidate will:

 

·        Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology, or similar Scientific Subject.

·        Have at least 5 years relevant experience in a pharmaceutical/healthcare environment.

·        Be very proficient in the use of Microsoft Word, Excel etc.

·        Have strong technical writing skills.

·        Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities.

·        Be a self-starter and capable of working on own initiative.

·        Strong teamwork skills.

·        Proven track record of meeting deadlines.

·        Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.


#LI-KV1
Requirements
Responsibilities include but are not limited to: · Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management. · Review and authorisation of Lab Data · Support Analytical Technical Transfer activity testing reports and documentation. · Document review/updates when required. · Equipment Calibration, Maintenance and Trouble Shooting. · Method Validation/Verification. · Training of QC Chemistry Laboratory colleagues. · Laboratory Investigation support · Laboratory Housekeeping and maintaining GMP standards. · Assisting in regulatory audits. The successful candidate will: · Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology, or similar Scientific Subject. · Have at least 5 years relevant experience in a pharmaceutical/healthcare environment. · Be very proficient in the use of Microsoft Word, Excel etc. · Have strong technical writing skills. · Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities. · Be a self-starter and capable of working on own initiative. · Strong teamwork skills. · Proven track record of meeting deadlines. · Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous. #LI-KV1
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