Supervisor, QO Finished Product (528077)

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.

Summary:

This supervisor is responsible for overseeing the day to day operations of the Quality Operations Finished Products group. The supervisor is also responsible for assisting in generating and controlling of raw material specifications of plasmatic products (as intermediates and/or final containers) and standard operating procedures relating to the group functions. In addtions this surpervisor is responsible for performing the final review of all inspection and packaging work orders. Furthermore the supervisor is also responsible for the initial evaluation and investigation of incidents related to returned goods and shipping incidents.

Primary responsibilities for the role:

• Schedule and supervise quality functions during 100% visual inspection and packaging operations of final container products inspection and release of intermediate products and imported finished products as well as other routine and non-routine functions assigned to the group including but not limited to label control retention sample maintenance and inspection
• Plan/analyze work flow delegate/prioritize tasks of the group
• Assist in writing and revising Raw Material Specification (RMS) and Standard Operating Procedures (SOPs).
• Gather data for routine Key Performance Indicators and also for statistical analysis for various projects.
• Perform the initial assess and investigation as required on product damage reports return goods reports and shipping incident reports.
• Assist investigations of deviations
• Issue update and maintain the database and log books routinely and coordinate equipment calibration and preventive maintenance
• Maintain a quality presence to ensure compliance with all regulatory requirements maintain current knowledge of regulatory and industry standards and participate in regulatory and internal inspections/audits as needed
• Provide guidance and hands-on training to direct reports. Coach counsel address complaints and resolve employee related issues with the collaboration of Human Resources.
• Involve in interviewing/selection process of hiring or promoting department personnel appraise and monitor performance of direct reports and provide a leadership role ensuring employee health and safety.

Knowledge Skills and Abilities:

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

Education/Experience:

• Bachelors Degree in Biology Chemistry Chemical Engineering or closely related scientific discipline is required.
• Minimum of 5 years related experience in a pharmaceutical GMP or FDA regulated environment is required.

Occupational Demands:

Must lift 50 lbs. Ability to stand for extended periods - up to four (4) hours at a time.

The estimated pay scale for the Supervisor Quality Operations Finished Product role based in Los Angeles California is $75334 to $110000 per year. We offer a wide variety of benefits including but not limited to: Medical Dental Vision PTO up to 5% 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 and may change over time. It is not intended as an exhaustive description of the job. Other duties may be assigned and qualifications required may change.

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; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy childbirth or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws including but not limited to the California Fair Chance Act the Los Angeles County Fair Chance Ordinance for Employers and the City of Los Angeles Fair Chance Initiative for Hiring Ordinance.

Location:NORTH AMERICA : USA : CA-Los Angeles:USCOI - City of Industry CA

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