Cgmp Jobs in Mexico

The Quality Systems Manager (QS Manager) ensures Quality is incorporated into the foundations of everything we do and through the life cycle of the products we create. This individual manages the design, creation, publication, and maintenance of the procedures, processes, and programs More...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you More...

Our client, a world leader in life sciences and diagnostics, is looking for the new role of Senior Lab Technician. Please have a look at the details below and let us know if you are interested. Job Title: Senior Lab Technician - DNA Amplification and PurificationDuration: Long-term C More...

Laboratory Support Technician IIWe are looking for a Lab Support Technician II to join our team.The Lab Support Technician II will ensure that all Buildings are cleaned and all equipment (tanks, buckets and bottles) used in the manufacturing of SLI products are cleaned and stored prop More...

We are working with a medical device client who is seeking a senior engineer to work on a range of validation initiatives related to new product introductions, transfers, and other related initiatives. This role will work on cross-functional projects, and is also an expert in validat More...

Job Description:Job Title : Validation Engineer,Job Location : Lincoln, RI,Job Type : Full-time roleSalary : 110K/AnnumValidation EngineerSeeking a capable Validation Engineer to work in the RI area. Ideal candidates would have previous experience supportin More...

This Associate Scientist II requires an analytical chemistry background and experience with Good Manufacturing practices (cGMP). Quality control testing is conducted on semi-solids (creams, ointments, lotions, gels, etc.), liquids, and suspensions products.Raw Material testing is cond More...

Job Details : Industry:- Automation & ValidationPosition:- Automation EngineerLocation: West Point-PA Duration:- 1 year Contract Description: DAY-TO-DAY:Perform automation and instrumentation and control engineering design services for existing facility projects, including More...

Send Your Resume On Hr WhatsApp Number +91-Manufacturers pharmaceuticals, including liquids, tablets, and drug Works closely with the laboratory manager and other pharmaceutical Collaborates with the quality assurance (QA) and quality control (QC) Sterilizes all equipment and keeps a More...

The Director of Operations is accountable for meeting production demand that supports corporate top-line revenue while improving efficiency to bottom-line This position is responsible for all day-to-day manufacturing operations, including purchasing, production planning, manufactur More...

MakroCare |A MakroGroup Company|MakroCare is an Expert Strategic Development and Commercialization Global Partner for the Pharmaceutical, Biotechnology and Medical Device Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning &a More...

My client is one of the top leading biopharma companies in the UK with the purpose to impact positively in global health and provide a workplace where people feel inspired and challenged to be the best they can be valued, and ;We have an exciting opportunity for a well-detailed and co More...

MUST ALREADY LIVE IN OR COMMUTABLE TO MANCHESTERPay Rate100000-125000Other Compensation15% bonus potentialThe QA Manager manages all quality systems including supplierdevelopment, calibration, internal auditing, NCMR, CAPA, qualityengineering, production support efforts including The More...

Job Title: Senior R&D ScientistJob Type: Full-Time, PermanentLocation: Toronto, Ontario, CanadaAbout the Company:Our client is a cleantech company that specializes in disruptive renewable plant-based chemistry, materials and products. Our client sources sustainable, new carbon mat More...

Seeking a Quality Assurance Engineer for a premier manufacturer, packager, and distributor of over-the-counter pharmaceutical products and consumer healthcare goods based in Copiague, NY. The ideal candidate has 3+ years Quality Assurance experience with a minimum of 2 years in the ph More...

Responsibilities: Issuance, update, and control of master batch records. Issuance of operational copies of manufacturing batch records to production. Performs cGMP & GDP review of finished production batch records. Check right first time and accuracy of data in the batch recor More...

Overview:The QC department is responsible for microbiological and analytical cGMP testing of sterile injectable products, raw materials, components and utilities. This includes routine microbiological and analytical testing of products for release and stability, development and valida More...

Responsibilities: Review all products PMs including leaflets, boxes, and aluminum foils for new products to comply with approved designs Determine color ranges for printed boxes for all ALJP products as per approved artwork Review ISO proof print orders as per technical agreement w More...

Our client, a world leader in Pharmaceuticals and In- Vitro Diagnostics (IVD) tools,is looking for Product Owner/Manager - Post Market Quality(100% Remote).Job Title: Product Owner/Manager - Post Market Quality(100% Remote)Job Duration: Long Term Contract (Possibility Of Further Ext More...

3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes2. Is this role 100% onsi More...