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Ehs In Pharma Jobs in California (NOW HIRING)

Socket.dev

Director, QC & Microbiology

San Diego, CA · On-site

$151 - $189/hr

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our ... EHS policies and procedures. * Embodies PCI Pharma Services cultural values and aligns daily ...

Zoetis Spain SL

Site Procurement Lead

Buellton, CA · On-site

$99 - $151/hr

In addition to the site procurement responsibilities, this role will take a lead in developing ... EHS, GMT, R&D and all functions that affect the supply base. Resources Managed Financial ...

EnduroSat

Facility Manager

Los Angeles, CA · On-site

$130K - $170K/yr

Taking on broader facilities ownership as the site matures - maintenance, EHS, capacity planning ... Background in aerospace/defense, semiconductor, data center, biotech/pharma GMP, or medical device ...

EnduroSat

Facility Manager

Los Angeles, CA · On-site

Taking on broader facilities ownership as the site matures -- maintenance, EHS, capacity planning ... Background in aerospace/defense, semiconductor, data center, biotech/pharma GMP, or medical device ...

EnduroSat

Facility Manager

Los Angeles, CA · On-site

$130 - $170/hr

Taking on broader facilities ownership as the site matures -- maintenance, EHS, capacity planning ... Background in aerospace/defense, semiconductor, data center, biotech/pharma GMP, or medical device ...

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Ehs In Pharma information

What is the difference between Ehs In Pharma vs Safety Officer in Pharma?

AspectEhs In PharmaSafety Officer in Pharma
CertificationsNEBOSH, OSHA, ISO 45001NEBOSH, OSHA, ISO 45001
Work EnvironmentManufacturing plants, laboratories, warehousesManufacturing plants, laboratories, warehouses
Primary FocusEnvironmental compliance, health & safety policiesWorkplace safety, accident prevention
Employer & Industry UsagePharmaceutical manufacturing companies, biotech firmsPharmaceutical manufacturing companies, biotech firms

Both Ehs In Pharma and Safety Officer in Pharma roles require similar certifications and work in comparable environments. While Ehs In Pharma emphasizes environmental management alongside health and safety, Safety Officers primarily focus on workplace safety and accident prevention. Both positions are integral to maintaining compliance and ensuring employee safety in pharmaceutical industries.

Is EHS in pharma a stressful job?

EHS in pharma can be stressful due to the responsibility of ensuring compliance with strict safety and environmental regulations, often involving audits and incident investigations. The role requires attention to detail, risk assessment skills, and sometimes working under tight deadlines, but it also offers a structured environment with safety protocols in place.

Is an EHS career in high demand?

Environmental, Health, and Safety (EHS) professionals in the pharmaceutical industry are in growing demand due to increasing regulatory requirements and a focus on workplace safety. EHS roles often require knowledge of safety protocols, compliance standards, and certifications such as OSHA or NEBOSH, making them a stable career choice with good job prospects.

What is EHS in pharma industry?

EHS in the pharma industry stands for Environment, Health, and Safety, focusing on ensuring compliance with regulations, maintaining a safe workplace, and minimizing environmental impact. EHS professionals develop safety protocols, conduct risk assessments, and promote a culture of safety among employees, often requiring certifications like OSHA or NEBOSH.

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For Ehs In Pharma jobs in California, the most frequently searched job titles are:

What job categories do people searching Ehs In Pharma jobs in California look for?

The top searched job categories for Ehs In Pharma jobs in California are:

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Cities in California with the most Ehs In Pharma job openings:

Ehs In Pharma jobs near you

Manufacturing Operations Manager (Tablet manufacturing)

Nivagen Pharmaceuticals

Pittsburg, CA • On-site

Full-time

Re-posted 11 days ago

Job description

Company
Nivagen pharmaceuticals Inc. located in Sacramento CA, we are engaged in the development, acquisition and sales of generic prescription drugs and over the counter products for the North American market. Our vision is to deliver high-quality products at affordable prices by leveraging global partnerships with the best FDA approved manufacturing facilities across the world.
Nivagen is focused in three areas of product development: development/co-development, acquisition/in-licensing, and providing sales and marketing services.
Role Purpose:
Responsible for performing tasks to specifications related to oral solid pharmaceutical manufacturing. The process includes tablet manufacturing.
Key Duties & Responsibilities:
  • Responsible for hands-on operation of production equipment including but not limited to: Blenders, Tablet Press, High Shear Granulator, Tray Dryer, Fluid Bed Processing Units, Mixers, Pumps, Vacuum and Loading machines, Labeling machines, Imprinting machines, Sealers, Bottle filling machines, Cappers, Induction sealers as Production Supervisor / Team Lead to manufacture oral dosage forms in a cGMP manufacturing facility.
  • Draft and manage daily/weekly production schedule
  • Ensure compliance with regulatory requirements such as Good Manufacturing Practices (GMP), Occupational Safety and Health Administration (OSHA) guidelines, and Environmental Health and Safety (EHS) regulations. You will stay updated with industry regulations and implement necessary changes to maintain compliance.
  • Manage workload of all the technicians and support staff in various departments such as mixing, granulation, drying, blending, compression, coating, packaging, receiving and warehouse.
  • Coordinate with relevant functional groups to ensure adherence to the production protocol and target volume requirements. Collaborate with cross-functional teams, such as R&D, engineering, and quality control, to support product launches, process validations, and technology transfers.
  • Troubleshoot and investigate deviations, actively participate in process optimization, support QA and other functional groups during internal and external audits including FDA, and actively support change control process.
  • Draft SOPs, training manual, qualification documents, protocols, and other controlled documents.
  • Manage receiving and warehouse personnel, inventory management, and ordering of supplies.
  • Performs all job duties in compliance with current Good Manufacturing Practices (cGMPs), following Nivagen Pharmaceuticals Quality Manual and Facility Standard Operating Procedures (SOPs).
  • Records all pertinent operations in packaging records, logbooks, and controlled documents.
  • Performs assembly, disassembly, operation, and cleaning of production and equipment.
  • Assists in routine preventive maintenance of all the utilities, production and packaging equipment.
  • Cleans and maintains production environments.
  • Performs line clearances prior to initiation of production orders to ensure materials and documents pertaining to the previous order have been appropriately removed from the production area.
  • Promote a culture of continuous improvement by encouraging suggestions and ideas from the team, implementing best practices, and monitoring key performance indicators (KPIs) to drive operational excellence.

Education
  • Requires Bachelor's Degree with 5 to 10 years in the pharma/Nutraceutical/Supplement environment
  • Requires experience with and an in-depth knowledge of cGMP regulatory requirements as they relate to the production of pharmaceutical products
  • Must be able to operate pharmaceutical manufacturing machinery
  • Solid mechanical aptitude and troubleshooting skills
  • Must have excellent communication skills
  • Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements, GMP
  • 5 to 10 years in Pharmaceuticals production

Technical competencies
  • Excellent written and verbal communication skills
  • Excellent math skills
  • Ability to read and comprehend SOP's, Batch Records and training documents.
  • Ability to multi-task effectively
  • Excellent interpersonal skills and ability to effectively interact with different functional groups

Apply