QC Sampler
* Morpeth, Northumberland
* Contract
* Expired
* Competitive
Job Overview
To perform and lead comprehensive sampling and inspection related tasks within the department. Be able to obtain a representative sample from each batch of material to establish whether the quality complies with the specification.
Demonstrate the techniques associated with sampling the types of materials received at Morpeth (solids, liquids, aseptic technique).
Demonstrates an authoritative knowledge of specific department operations, and has significant interaction with other associated departments in order to communicate any relevant information relating to the material.
Understands the principles and activities involved with NIR testing and analysis, relating to system operation and establishing reference libraries, whilst further maintaining and developing the system.
Key Responsibilities
1. Able to sample raw material, intermediate, API or drug product to GMP standards using the appropriate equipment within the allocated turnaround time to support product processes.
2. Ensure compliance with current GMP / GLP’s as required by regulatory and Company directives and Health and Safety e.g. COSHH.
3. Able to communicate any potential issues so as to minimise production delays.
4. Knowledge of site systems and GMP requirements; OOS procedure, Deviation Reporting, Trackwise etc.
5. Liaise with other departments within the organisation to support QC operations.
6. Display Winning Behaviors at Morpeth.
7. Works in a manner to support key quality performance targets e.g. Raw Material release turnaround, Deviation and Commitment Tracking Actions.
8. Supports Continuous improvement initiatives.
9. Contributes to and supports quality, including out of specifications, and safety investigations to resolve issues and prevent re-occurrence.
MS Project, MS Word, MS Excel, email and verbal communication skills.
Equal Employment Opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms.
We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited.
Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.
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