Pharmaceutical jobs in Sacramento, California - Page 2Create job alerts

Job Description About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to the core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals 3900 Duckhorn Dr, Sacramento, CA 95834. About the Job: Title of the Position: Automation Technician The Automation Technician ensures reliable operation of sterile pharmaceutical manufacturing systems by installing, maintaining, calibrating, and troubleshooting automation components, process instrumentation, drives, motors, control devices, clean utility systems, and aseptic production equipment. The role supports continuous and compliant operations under cGMP, FDA 21 CFR Part 11, and cleanroom standards. Responsibilities: • Install, maintain, calibrate, and troubleshoot sensors and transmitters for pressure, temperature, flow, level, pH, conductivity, and environmental monitoring., • Support in performing GMP‑compliant calibrations with complete traceability and accurate documentation., • Install, maintain, and troubleshoot motors, pumps, fans, drives, control devices, and sterile manufacturing equipment., • Perform conduit bending, cable routing, wire pulling, cable termination, tray installation, and equipment connections in accordance with plant procedures., • Install and modify control panels, junction boxes, and instrumentation assemblies., • Diagnose issues in circuits, protection components, sensors, actuators, drives, and automated machines., • Use diagnostic tools such as multimeters, clamp meters, insulation testers, and calibration instruments., • Support PLC, HMI, SCADA, BMS, and EMS platforms, including troubleshooting and system checks., • Conduct loop checks, functional tests, FAT/SAT, commissioning, and support validation activities (IQ/OQ/PQ)., • Maintain and troubleshoot systems for PW, WFI, Clean Steam, CIP/SIP, HVAC/HEPA controls, and aseptic filling/packaging operations., • Read and interpret P&IDs, wiring diagrams, schematics, ladder logic, and loop drawings., • Maintain cleanroom support systems, including differential pressure controls, HEPA filtration, and environmental monitoring., • Ensure compliance with cGMP, cleanroom classification requirements, FDA 21 CFR Part 11, and data integrity principles., • Perform preventive, corrective, and predictive maintenance., • Conduct root‑cause analysis and implement CAPA actions., • Ability to work rotating, weekend, or extended shifts., • Exposure to high‑noise areas (PPE provided)., • Frequent work on mezzanine floors, elevated platforms, ladders, and step‑ups., • Work inside aseptic cleanrooms and controlled environments (ISO 5/7/8) wearing full gowning., • Exposure to hot, cold, humid, or pressurized utility systems such as PW, WFI, Clean Steam, and HVAC units., • Occasional work in tight spaces, behind panels, or equipment enclosures., • Regular use of PPE, including sterile gowning, gloves, and eye protection. Education: Minimum 5 to 10 years of professional experience in the field of pharmaceutical or manufacturing industry. Knowledge, Skills, and Abilities: Functional: • Strong troubleshooting skills across sensors, transmitters, motors, drives, actuators, control components, automated machinery, and process systems., • Experience with conduit bending, tray installation, cable pulling, wire routing, cable dressing, and termination., • Proficiency in installing and modifying panels, junction boxes, and equipment assemblies., • Skilled in using multimeters, clamp meters, insulation testers, and calibration devices., • Ability to install, connect, and terminate control wiring and instrument cabling for field devices., • Understanding of circuits, drives, starters, protection components, actuators, and control system diagnostics., • Ability to read and interpret P&IDs, schematics, wiring diagrams, ladder logic, and loop documentation., • Knowledge of GMP requirements, sterile manufacturing, cleanroom practices, aseptic operations, and validation processes., • Strong documentation discipline, attention to detail, and audit readiness., • Result oriented, • Innovative thinking, • Time Management, Professional Work Conduct at all times, • Problem-solving ability & High level of self-motivation, • Strong interpersonal relationship skills, • Valid driver's license and acceptable driving record, • Legally authorized to be employed in the United States, • Competitive Salary: $70,304 - $80,000, • Yearly bonus eligibility, • Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being, including medical, dental, and vision coverage, • Paid time off plan Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.

The Associate Director of Quality Operations will spearhead initiatives focused on operational excellence, robust risk management practices, and the optimization of global quality system processes within a diverse organization.This pivotal role is essential in ensuring the efficiency, compliance, an

Pharmaceutical Maintenance Technician. Pharmaceutical Maintenance Technicians.

Minimum of 10 years of experience in Medical Affairs, Medical Communications, or Publication Planning within the pharmaceutical or biotechnology industry. Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Location: Oakland, Pleasanton, Sacramento (Must be in Northern California).Bachelor's degree + 5+ years of data analysis/management/migrations experience.Expert level MS Excel Data Analyst background ability to gather data, cleansing data, standardizing data sets.

Otsuka Pharmaceutical Development & Commercialization, Inc. The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the impact of regulatory changes to the pharmaceutical environment. Oversee the capt

This is a W2 role with base salary, uncapped commission, and a monthly car allowance.This is a performance-driven role for someone who thrives in an entrepreneurial environment and wants to be.Can reside in San Francisco, San Jose or Sacramento.Drive prescription growth with targeted specialty HCPs.

Chemistry, Biology, Pharmaceutical Sciences); advanced degree preferred. Minimum 12 years of experience in pharmaceutical quality assurance or quality systems, with at least 5 years in a global leadership role. Otsuka America Pharmaceutical Inc.

Pharmaceutical Maintenance Technician. Pharmaceutical Maintenance Technicians.

A minimum of ten years in pharmaceutical manufacturing, quality assurance, or quality control roles, with experience in managing quality oversight.

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Congress ; or 5+ years diverse background in the pharmaceutical industry, with at least 5 years in government affairs required. In depth understanding of healthcare, pharmaceutical and biotechnology industry issues required. Otsuka America Pharmaceutical Inc.

The Director of GxP Training is a pivotal leader in the Learning Center of Excellence under Global Quality.This role focuses on creating and implementing a global GxP training strategy that ensures compliance with regulatory standards and fosters a robust quality culture within the organization.The

Minimum of 10 years of pharmaceutical experience, with a strong understanding of sales force operations and execution. Established expertise in business analytics, business operations, sales support, and resource management within a commercial pharmaceutical organization. Otsuka America Pharmaceutic

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Otsuka Pharmaceutical Development & Commercialization, Inc. A minimum of 10 years in the pharmaceutical industry with a solid grounding in drug development processes, particularly within relevant therapeutic areas such as psychiatry or neurology. If you are a visionary leader ready to make an impact

Otsuka Pharmaceutical Development & Commercialization, Inc. Explore and analyze common pharmaceuticals data (e. Otsuka America Pharmaceutical Inc.

Over 10 years of experience in pharmaceutical, biotech, or healthcare consulting, specializing in HEOR, RWE, and market access strategy.

Ten years of combined and/or pharmaceutical manufacturing, QA or QC assurance roles managing and directing quality oversight of commercial product and development project activities. Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

The Director of Medical Strategy in Rheumatology and Dermatology plays a pivotal role in shaping the strategic planning processes for early development assets in the Nephrology and Immunology portfolio.This role demands a proactive and flexible approach, balancing a diverse array of priorities as we

Within Otsuka Pharmaceutical Co. Otsuka Pharmaceutical Development & Commercialization, Inc. A minimum of 10 years of experience in the pharmaceutical industry, extensive working knowledge in the drug development process with proven progression in relevant R&D roles and significant experience in rel

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

The Associate Director of Good Practice (GxP) Training plays a vital role in the Learning Center of Excellence within Global Quality.This position is essential for crafting and sustaining effective training programs that uphold compliance with GxP regulations across the organization.As a leader in t

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Minimum of 5+ years of relevant experience in the pharmaceutical industry, with strong preference for experience in Clinical Development, Research, or Medical Affairs. Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

We focus on pharmaceuticals that address complex diseases, particularly in Neuroscience, Nephrology, and Immunology. Collaborating closely with Otsuka America Pharmaceutical, Inc. Minimum of five years of experience in clinical research within the pharmaceutical industry or academia.

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Minimum of 7 years of pharmaceutical experience. Proven experience in data analysis, business intelligence, and strategic planning within a pharmaceutical sales environment. Otsuka America Pharmaceutical Inc.

The Associate Director will play a critical role within the Learning Center of Excellence in Global Quality, focusing on the design, implementation, and maintenance of impactful training programs for the Commercial and General & Administrative (G&A) functions.This position ensures that learning stra

A leading pharmaceutical company is seeking a Senior Director of Medical Communications.

At least 10 years of experience in Medical Affairs, Medical Communications, or Publication Planning in the pharmaceutical or biotechnology sector.

Join our dynamic team as the Director of Training Operations! This pivotal role is a senior leadership position within the Learning Center of Excellence (CoE) at Otsuka, where you will oversee global training management operations.Your expertise will ensure compliance with regulatory standards while

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

In pharmaceuticals, Otsuka focuses on the development and commercialization of therapies in the challenging areas of Neuroscience, Nephrology, and Immunology in addition to research programs in various unmet specialty disease areas. In conjunction with Otsuka America Pharmaceutical, Inc. The Senior

Minimum of 7 years of experience in Medical Affairs or Scientific Communications within the pharmaceutical or biotechnology industry. Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Minimum 5 - 7 years of experience in a regulated industry (pharmaceutical or medical device), with 3-5 years in pharmaceutical quality, with specific experience in controlled substances and commercial quality operations. Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commerci

Otsuka America Pharmaceutical Inc. Otsuka Pharmaceutical Development & Commercialization, Inc.

Minimum of 5+ years of relevant experience in the pharmaceutical industry, with strong preference for experience in Clinical Development, Research, or Medical Affairs.

A global pharmaceutical company is seeking a Medical Director for Rare Disease to shape the strategic processes and planning for assets in development. Candidates should possess an advanced scientific degree and over 5 years of experience in the pharmaceutical industry, particularly in clinical deve

A leading pharmaceutical company is seeking a Medical Director for its Rare Disease portfolio. The ideal candidate will have an advanced scientific degree and over 5 years of relevant experience in the pharmaceutical industry.