- Nestle (San Antonio, TX)
- …time. + Perform all functions according to Good Manufacturing Practices ( cGMP ) and company Standard Operating Procedures (SOP) meeting required production standards. ... + Fully trained and qualified in all operating instructions, SOP's, JHA, and area specific technical instructions for assigned role + Perform warehouse transactions into inventory tracking software (AS400) + Prepare, load and receive shipments of raw materials… more
- Otsuka America Pharmaceutical Inc. (Austin, TX)
- …techniques, bioreactor operations, and cell line development + Strong knowledge of cGMP regulations and ICH guidelines relevant to upstream biologics manufacturing + ... Experience with a variety of expression systems (eg, CHO, HEK293, microbial) + Familiarity with Quality by Design (QbD) principles and their application to upstream processes + Excellent leadership skills with the ability to mentor and develop team members +… more
- dsm-firmenich (Freeport, TX)
- …of data analysis techniques, Root Cause Analysis, tools and application. + cGMP operational knowledge considered a plus. + Solids and dust handling knowledge ... considered a plus. At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A… more
- Fujifilm (College Station, TX)
- …Work with Quality management to implement quality systems that will enable cGMP manufacturing of pre-clinical to commercial products + Responsible for Manufacturing ... audit preparations, conducting internal audits, assisting client audits with site documentation collation + Coordinate batch and formulation record review and corrections to executed records. + Coordinates the initiation of new deviations. + Leads deviation,… more
- BioBridge Global (San Antonio, TX)
- …control operations and eQMS. Must maintain knowledge of ISO Standards, cGMP (current Good Manufacturing Practices) and regulatory requirements concerning creation ... and maintenance of controlled documents and record retention. Must have working knowledge of a microbiology laboratory. Must have working understanding of aseptic or sterile behavior and techniques. Must have a working knowledge of various LIS software… more
- BioBridge Global (San Antonio, TX)
- …according to organizational and regulatory (NMDP, AABB, FACT, ISO, FDA, and cGMP ) standards. Assist with validation of all procedures performed thus providing for ... the safety and efficacy of products to include preventative maintenance. Attend meetings, seminars, and other workshops as required. Maintain a close working relationship with management keeping them informed on issues pertaining to laboratory functions.… more
- Kedplasma (Pharr, TX)
- …Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make your job ... description as complete as possible. However, that in no way states or implies that these duties/responsibilities are the only duties you will be required to perform. The omission of specific duties/responsibilities does not exclude them from the position if… more
- Bio-Techne (Austin, TX)
- …Office + Familiarity with ERP systems, particularly QAD a plus + Knowledge of cGMP , GLP, ISO, CE or other regulated environments a plus **Why Join Bio-Techne:** **We ... offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase… more
- Charles River Laboratories (Houston, TX)
- …completing all service and compliance documentation as required by company policy, cGMP and FDA. * Responsible for resolving client testing laboratory instrument ... service issues. **Job Qualifications** The following are **minimum qualifications** related to the **Instrument Field Support Specialist** for our Nexus Robot and Endosafe range: Qualification in Engineering, Chemistry, Microbiology, Biology or equivalent… more
- General Atomics (El Paso, TX)
- Diazyme, an affiliate of General Atomics, is a cGMP and ISO 13485 certified medical device manufacturer. Diazyme uses its proprietary enzyme technologies to develop ... diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Their products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes. With… more