Top 3 Manufacturing program manager Jobs in Smyrna, De

Assistant Manager of Quality
CSL Plasma —Dover, DE
- Full-time
- 5 years
- Mid-level
- Clinic
Plant Engineering Manager
Ardagh Group —Bridgeton, NJ
- $110,900 - $166,300 a year
- 5 years
- Engineering
- Continuous improvement
- Paid holidays
- Disability insurance

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Phase I Supervisor
Laurel Valley Farms —Landenberg, PA
Assist with compost projects, contractor coordination, and operational improvement initiatives as assigned. Maintain accurate process and operational records…
$70,000 - $80,000 a year
Quick Apply
12d
Sr. Corporate Account Manager, Personal Care Manufacturing - Industrial Hygiene Solutions
Ecolab Inc. —Philadelphia, PA
Knowledge of field sales and proven ability to collaborate and partner with this team. This role reports to the Global Corporate Accounts VP with significant…
$153,300 - $229,900 a year

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Production Program Manager, Manufacturing
Anduril Industries —Ashville, OH
In this role, you will plan, analyze, and report on program status, master technical concepts, mitigate risks, and align cross-functional teams to drive mission…
$128,000 - $171,000 a year
Quick Apply
7d
Validation Engineer Supervisor
Hendrickson —Hebron, OH
Lead and manage the testing, development, validation, and sign off of all major product programs; proliferation of existing products into specialty market…
Quick Apply
2d

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Assistant Manager of Quality

CSL Plasma -
Dover, DE

Apply Now

Job Details

Full-time

Qualifications

Supervising experience
Bachelor's degree
Manufacturing company experience
Quality assurance experience within healthcare

Full Job Description

Entity: CSL Plasma

Job Category: Quality

Job Family: Plasma Center

Job Type: Full Time

Location: Dover, Delaware, United States

Employer Reference: R-284225

Job Description

Responsibilities:• Ensure center is “inspection ready” at all times by managing adherence to Standard Operating Procedures (SOPs), compliance policies and the quality system, utilizing sound Quality principles, self-inspection learnings, non-conformity discovery and appropriate remediation. Prepare regular reports to center, area and corporate quality management as to the state of quality and systems at the center.• Manage site Quality Control program including but not limited to calibrations management, monitoring of compliance to defined processes e.g. sampling, competency checks, Key Performance Indicators (KPIs), trending and analysis of KPIs, root cause and failure mode impact assessment and change management.• Lead and develop direct reports ensuring they are competently skilled to perform their QA roles. Lead by example; consistently motivate staff through education to high levels of competency that drive success in a dynamic and regulated environment. Upon proper review with center and quality management, recruit, hire, conduct performance reviews and enact corrective actions, up to and including termination.• Participate with management to develop programs and methods to streamline center processes resulting in improved customer/donor service, product yields and financial results while maintaining compliance and quality.• Receive and provide feedback to staff on observations leading to improved adherence to GMP standards. Report concerns or deficiencies to area personnel and/or area management immediately. Make recommendations for remedial actions to resolve audit observations and other non-compliance issues of deficiencies.• Lead and function as the key quality representative for site supplier, customer and regulatory audits. Lead center review of findings, coordination of remediation (CAPA), if needed and successful closure of timely audits. Utilize quality tools and applications to facilitate understanding of issues and documentation.• Maintain clean efficient work environment and ensure sufficient operating supplies and availability of forms, as needed. Comply with all Health Safety and Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Conduct routine audits of internal procedures and documentation, as necessary. Promote safety in all actions.• Adhere to all HR policies and practices through fair and equitable treatment of all employees. Communicate effectively with HR to ensure HR compliance and ensure center management is doing the same.• Comply with all federal, state and local regulatory and company policies and procedures.• Responsible for notification to the ADOQ for any event that negatively affects the safety, quality, identity, purity or potency of the product that results in pausing or disruption of business. If necessary, notification must be elevated to any of the following, Regional Director, Associate Director of QA, Divisional Director or Director of Quality Systems and Assurance.• Maintain confidentiality of all personnel, donor and center information. Understand policies and procedures associated with hyper immune programs at the center if applicable.• Lead investigations into deviations to determine root cause, correction/preventative actions and effectiveness checks. Monitor CAPA’s and effectiveness checks to ensure issues are resolved.Qualifications:• Bachelor degree in scientific discipline/life sciences or related discipline• 5+ years' experience related to quality and regulatory/ Plasma industry experience• Demonstrated leadership/supervisory experience• Knowledge of government and industry regulationsDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

About CSL Plasma

CSL Plasma operates one of the world's largest and most sophisticated plasma donation networks, with nearly 330 donation centers in the U.S. and Europe. CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL (ASX:CSL; USOTC:CSLLY), headquartered in Melbourne, Australia, employs 29,000+ people. For more information about CSL Plasma visit, https://www.cslplasma.com/.

Our Benefits

For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

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manufacturing program manager jobs in smyrna, de

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Job Description

About CSL Plasma

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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