Supervisor, Manufacturing (Coagulation Filling)

Grifols; Los Angeles (CA); On-site; USD 90,000 - 98,000; Full time

Job summary

Grifols is seeking a Supervisor for their Manufacturing department in Los Angeles. This role involves overseeing the production process, ensuring compliance with GMP regulations, and developing department staff. The ideal candidate will possess strong leadership and analytical skills and have experience in a regulated environment. If you are looking for a rewarding opportunity in the healthcare industry, this could be your next challenge.

Benefits

Medical, Dental, and Vision insurance

401(k) match up to 8%

Tuition reimbursement

Paid Time Off (PTO)

Qualifications

• Minimum 2 years of experience in a pharmaceutical or FDA regulated environment.
• In-depth understanding of GMPs and regulatory standards.
• Prior supervisory or leadership experience preferred.

Responsibilities

• Oversee the manufacturing process and personnel on designated shift.
• Participate in troubleshooting processes and maintain product quality.
• Generate reports on significant events or issues within production.

Skills

Leadership

Problem Solving

Organizational Skills

Analytical Skills

Interpersonal Skills

Education

Associate's Degree (preferred)

Bachelor's Degree in Biology, Chemistry or related field

Tools

MS Office

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

POSITION SUMMARY

The Supervisor, Manufacturing, oversees the manufacturing process and the department personnel on designated shift to ensure process meets cGMP (current Good Manufacturing Practices) and company standards for an aseptic operation . Trains and develops department technicians.

ESSENTIAL DUTIES & RESPONSIBILITIES may include the following. Other duties may be assigned.

• Provides immediate supervision to a unit or group of employees, assigning tasks, checking work at frequent intervals, and maintaining schedules.

• Oversee production review of all department batch documentation for completeness and accuracy.

• Initiate Facility Work Orders when equipment requires repair.

• Participate in process/product troubleshooting in order to correct/maintain aseptic processing and desirable product yields, as well as environmental control of facility.

• Recommend and implement measures to improve production methods, equipment performance, facility layout, and quality of product.

• Maintain a quality presence to ensure compliance with all regulatory requirements.

• Maintain current knowledge of regulatory and industry standards.

• Generate thorough written reports, when required , that summarize investigations performed for out-of-specification results or out-of-procedure events.

• Participate in regulatory and internal inspections/audits including providing written responses as applicable for area of responsibility.

• Provide guidance and hands-on training to direct reports.

• Appraise and monitor performance of department personnel.

• Coach, counsel, address complaints and resolve employee related issues with the collaboration of Human Resources.

• Provide a leadership role ensuring employee health and safety.

• Involved in interviewing/selection process of hiring or promoting department personnel.

REQUIRED EXPERIENCE/SKILLS & EDUCATIONAL QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required . Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

• Associate’s degree required . Bachelor's degree preferred. Emphasis in Biology, Chemistry, Chemical Engineering or closely related scientific / technical discipline is preferred.

• Minimum of 2 years of related experience in a pharmaceutical, GMP, or FDA regulated environment is required .

• Equivalency : In lieu of an Associate's degree, candidate must have a High school diploma or GED, and a minimum of 4 years of related experience in a pharmaceutical, GMP, or FDA regulated environment.

• Requires an in depth understanding of pharmaceutical manufacturing operations, including protein purification and aseptic processing.

• Comprehensive knowledge and understanding of cGMPs , FDA regulations, and industry guidelines.

• Prior supervisory or leadership experience is highly preferred.

• Demonstrated ability to inspire high performance in others and align team members around shared goals.

• Demonstrated leadership skills with the ability to motivate, guide, train, coach and develop department personnel.

• Demonstrated project management skills.

• Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.

• Must be proactive, results oriented, and have strong attention to detail.

• Self-starter with strong work ethic and the ability to exercise good judgment.

• Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.

• Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.

• Excellent verbal and written communication skills in the English language.

• Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint).

• Must be flexible with working hours / shifts in order to accommodate the 24 hour , 7 day plant operation.

PHYSICAL REQUIREMENTS

• Ability to lift /move up to 50 pounds.

• Ability to stand for extended periods - up to four (4) hours at a time.

• Manual dexterity to perform all job functions.

• Ability to gown and work in an aseptic/clean room environment.

• Exposure to toxic/caustic chemicals and biological hazards.

The estimated pay scale for the Supervisor, Manufacturing role based in Los Angeles, CA starts at $90,000 -$98,000 per year. Additionally, the position is eligible to participate in up to 8% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 8% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!

*This job description is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned and qualifications required may change over time.

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants, including those with arrests or conviction records, in a manner consistent with the requirements of applicable state and local laws, including the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.

Location:NORTH AMERICA : USA : CA-Los Angeles:USVALLEY - Valley Bl Mfg Plant - LA, CA

Learn more about Grifols