Training and Doc Control Specialist

Posted Yesterday
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95834, Sacramento, CA, USA
In-Office
Mid level
Pharmaceutical
The Role
Develops and delivers training for document control and QMS processes, manages training records and curriculum in the LMS, supports onboarding and change management, ensures compliance with ISO/FDA/GMP/GDP, and provides documentation and audit support.
Summary Generated by Built In

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, Sacramento, CA

3900 Duckhorn Dr, Sacramento, CA 95834

About the Job:

Title of the Position: Training and Document Control Specialist

The Document Control & Training Specialist will support the development, delivery, and maintenance of training programs related to document control, ensuring compliance with industry standards like ISO, FDA, GMP, or GDP. They ensure that employees understand and follow document control processes, systems, and regulatory requirements, while also supporting audits and quality management initiatives.

Responsibilities:

  • Training Development & Delivery: Design and create training materials for QMS and document control processes; deliver instructor-led and virtual sessions across departments and sites.
  • Onboarding & Change Management: Provide onboarding training for new hires on document management and QMS procedures; support change initiatives by coaching and training impacted teams.
  • Training Effectiveness: Evaluate training outcomes, update content, and ensure alignment with industry standards.
  • Compliance Support: Maintain training records, track completion and competency, and provide documentation for audits to demonstrate compliance.
  • Curriculum & Reporting: Create/add curriculum assignments in the training system, generate reports, and distribute training results.
  • Cross-Functional Support: Partner with other departments to provide first-line training support and improve training programs.

Qualifications:

  • Bachelor’s degree or equivalent combination of education and experience.
  •  3–5 years in a regulated industry; preferred experience in project management, training, quality systems, or related fields.

Knowledge, Skills, and Abilities:

  • Familiarity with regulatory standards (ISO, FDA, GMP, GDP).
  • Strong presentation, communication, and facilitation skills.
  • Problem-solving and proactive approach to challenges.
  • Excellent organization and attention to detail.
  • Proficiency in Microsoft Office and Learning Management Systems (LMS). 

Job Requirements:

  • The role involves working in both office and manufacturing environments, requiring adherence to safety protocols and GMP standards
  • Occasional travel may be required for audits, supplier evaluations, or training
  • Must live or be willing to move to the Sacramento Metropolitan Region (Approx. 40 miles’ radius)
  • Familiarity with regulatory standards (ISO, FDA, GMP, GDP).
  • Strong presentation, communication, and facilitation skills.
  • Problem-solving and proactive approach to challenges.
  • Excellent organization and attention to detail.
  • Proficiency in Microsoft Office and Learning Management Systems (LMS). 
  • Additional Information:

    • Flexibility is required as work hours and start times may vary to provide coverage on different shifts to meet business needs.
    • Overtime and weekend work may be required.
    • The individual must be available via cell phone (on-call).

Benefits:

  • Pay range Competitive
  • Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being
  • Medical, dental, and vision coverage
  • Paid time off plan
  • 401k savings plan

Additional Information:

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.

We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.

Skills Required

  • Bachelor's degree or equivalent combination of education and experience
  • 3-5 years' experience in a regulated industry
  • Familiarity with regulatory standards (ISO, FDA, GMP, GDP)
  • Experience developing and delivering training (instructor-led and virtual)
  • Proficiency in Microsoft Office
  • Proficiency in Learning Management Systems (LMS) and training record management
  • Strong presentation, communication, facilitation, organization, and attention to detail
  • Willingness to work in office and manufacturing environments and follow GMP/safety protocols
  • Must live in or be willing to relocate to the Sacramento metropolitan region (approx. 40-mile radius)
  • Flexibility for variable shifts, overtime, weekend work, and on-call availability via cell phone
  • Preferred: experience in project management, training, quality systems, or related fields
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The Company
HQ: Sacramento, California
122 Employees
Year Founded: 2009

What We Do

Nivagen is 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. Our sales and marketing personnel are among the best in the world. The US generic prescription market is currently at approximately $60 billion, and over $120 billion's worth of products will be coming off of patent protection in next 10 years. Nivagen believes that, with its strategic partnership model of global alliances with highly efficient pharmaceutical companies across the globe, we can provide cost savings to the consumer while creating value for all members of the supply chain. Nivagen is focused in three areas of product development: development/co-development, acquisition/in-licensing, and providing sales and marketing services. We are actively looking to partner with CRO and CRAM to co-develop products. We are also acquiring existing products. If you are small FDA qualified manufacturer and want to launch your company or product in the US, Nivagen can provide complete turnkey solutions and cost effective delivery on an accelerated timeline.

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