drjobs Supervisor, Manufacturing (Coagulation Filling) (528198)

Supervisor, Manufacturing (Coagulation Filling) (528198)

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1 Vacancy
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Job Location drjobs

Los Angeles, CA - USA

Yearly Salary drjobs

$ 90000 - 98000

Vacancy

1 Vacancy

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 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 . Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

  • Associates degree . Bachelors 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 .

  • Equivalency: In lieu of an Associates 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 $90000 -$98000 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 duties may be assigned and qualifications 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


Required Experience:

Manager

Employment Type

Full-Time

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