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- ...project requirements. Ability to read and interpret engineering plans and specifications. BSc degree in construction or engineering-related field from an accredited university, or an AS degree combined with industry experience. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedContract workFor contractorsWork experience placementWork at officeImmediate start
- ...Expertise in DeltaV, Building Management Systems (BMS), BAS, and Environmental Monitoring Systems (EMS). Strong knowledge of GAMP5, FDA regulations, and 21 CFR Part 11. Excellent technical documentation and project management skills. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedContract workWork experience placement
- ...commissioning/validating MES software platforms Exposure to FDA regulated environments including validation experience Understand 21 CFR Part 11, GAMP 5, and other regulatory guidance associated with computer/automation based systems #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedContract workWork experience placement
- ...pharmaceuticalenvironments. • Expertise in isolators, bioreactors, fume hoods, and other lab equipment. • Strong knowledge of regulatory requirements and risk-based validationapproaches. • Excellent project management and problem-solving skills. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedContract workWork experience placement
- ...metadata management tools. Familiarity with event streaming platforms like Kafka. Familiarity with modeling for structured and semi‑structured data. Certifications in cloud platforms (AWS, Azure, etc.) or database technologies. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedImmediate start
- ...independently and in a team setting, with the ability to effectively communicate cross-functionally Ability to support multiple concurrent projects in a fast-paced environment Strong interpersonal and relationship-building skills #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedFull timeWork experience placement3 days per week
- ...requirements and ensure project success. Candidates should have over 12 years of experience in SDLC methodologies, strong skills in C#, Python, and SQL, a deep understanding of middle office functions, and excellent communication skills. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedWork at office
- ...will possess over 10 years of experience in CQV roles within the pharmaceutical sector and a strong understanding of FDA regulations. This position offers the opportunity to lead crucial validation efforts in a dynamic environment. #J-18808-Ljbffr Pharmatek Consulting Inc.Suggested
- ...related field. 10+ years of experience in CQV roles within pharmaceutical or biotechindustries. Expertise in facilities, utilities, and building management systems (BMS). Strong understanding of FDA regulations and cGMP requirements. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedContract workWork experience placement
- ...Applicants should have over 10 years of relevant experience and a strong background in computerized systems validation. The role offers an opportunity to lead crucial validation activities within a project-oriented environment. #J-18808-Ljbffr Pharmatek Consulting Inc.Suggested
- ...industry standards. Ideal candidates have at least 10 years of experience in biotech and proficiency with Emerson DeltaV and Oracle tools. This position may require occasional flexibility in hours and offers a hybrid work environment. #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedLong term contract
- ...player with a strong work ethic. Ability to thrive in ahigh-intensity, fast-paced environment and prioritize/deliver multipleactive projects. Educational Requirements: An advanced degree from a top university is strongly desired #J-18808-Ljbffr Pharmatek Consulting Inc.SuggestedLong term contractPermanent employmentWork at office3 days per week
- ...engineers. Ideal candidates will have over 10 years of experience in database architecture and must be skilled in relational and cloud-based databases. The position is on-site, preferably located in San Antonio or Plano, Texas. #J-18808-Ljbffr Pharmatek Consulting Inc.Suggested
- ...include collaborating with stakeholders, managing project documentation, and ensuring GMP compliance. This on-site position requires strong interpersonal skills and the ability to manage multiple projects in a fast-paced environment. #J-18808-Ljbffr Pharmatek Consulting Inc.Suggested