Top 126 Senior manufacturing associate Jobs in Elkridge, Md

Associate II, Manufacturing
Catalent —Harmans, MD
- $31.25 - $36.05 an hour
- Overtime
- English
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
10d
Associate I, Manufacturing
Catalent —Harmans, MD
- $26.44 - $31.25 an hour
- Overtime
- English
- High school diploma or GED
- Assembly
- Paid holidays
- Health insurance
10d
Senior Associate Attorney
Family Legal Advocacy Group, LLC —Columbia, MD
- $90,000 - $120,000 a year
- Full-time
- Hybrid work
- Mid-level
- In-person
- 2 years
- Opportunities for advancement
Quick Apply
Senior Registered Client Service Associate - Hunt Valley, MD
Raymond James Financial, Inc. —Hunt Valley, MD
- $45,000 - $85,000 a year
- Full-time
- High school
- Writing skills
- Mid-level
- Paid holidays
- Health insurance
Community Health Worker [Senior Associate] - Maryland
Medicalincs, LLC —Silver Spring, MD
- Overtime
- Hybrid work
- School experience
- Spanish
- Customer service
Quick Apply
Research Associate, Assay V&V and Reagent Manufacturing Scale-Up
Novel Microdevices Inc. —Baltimore, MD
- $70,000 - $80,000 a year
- Full-time
- Bachelor's degree
- Quality control
- No travel
Quick Apply
6d
Associate Producer, Photo and Video
Erickson Senior Living —Baltimore, MD
- $50,000 - $53,000 a year
- 18 years or older
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
Associate, Strategic Marketing
Erickson Senior Living —Baltimore, MD
- $60,000 - $65,000 a year
- 18 years or older
- Microsoft Outlook
- Sales
- Free parking
- Health insurance
6d
Senior Accounting Associate, Aerospace, Defense, and Government
Aprio —Baltimore, MD
- $90,000 - $125,000 a year
- Full-time
- Remote
- Customer service
- Mid-level
- Bachelor's degree
- Profit sharing
- Wellness program
Sr. Clinical Research Associate
Emmes Group —Rockville, MD
- Full-time
- Bachelor's degree
- Travel
- Organizational skills
Associate - Quality Control
Accu-Tech —Hanover, MD
- $21.04 - $25.26 an hour
- Full-time
- Microsoft Outlook
- Word processing
- English
- Health insurance
- Dental insurance
3d
Business Development Sr. Associate
Johns Hopkins Care at Home —Baltimore, MD
- $49.01 - $78.43 an hour
- Full-time
- 5 years
- Finance
- Analysis skills
Senior Associate Appraiser
Cushman & Wakefield —Baltimore, MD
- $59,585 - $70,100 a year
- Full-time
- Microsoft Outlook
- Analysis skills
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
Sr Development Associate
Leaders of Tomorrow Youth Center —Owings Mills, MD
- $40 an hour
- Part-time
- Microsoft Word
- Customer service
- Research
- Work from home
Production Associate - HV
Used Cardboard Boxes Inc. —Hunt Valley, MD
- From $17 an hour
- Full-time
- Ability to lift 50 pounds
- Entry level
- Opportunities for advancement
Quick Apply
Operations Associate
Blind Industries and Services of Maryland —Baltimore, MD
- $15 - $17 an hour
- Full-time
- Ability to sit for extended periods
- Manufacturing
- Ability to stand for extended periods
- Profit sharing
- 403(b) matching
Senior Associate, Clinical Trials & Corporate Contracts
University of Maryland, Baltimore —Baltimore, MD
- $76,000 - $86,000 a year
- Full-time
- Hybrid work
- Mid-level
- Analysis skills
- 1 year
- Paid holidays
- Health insurance
Sr Associate Product Manager
McCormick —Hunt Valley, MD
- $74,330 - $130,080 a year
- Marketing
- Merchandising
- Mid-level
- Profit sharing
- Paid parental leave
6d
Associate Healthcare Director/Assistant Director of Nursing
Harmony Senior Services —Bowie, MD
- Weekends as needed
- CPR Certification
- Nursing
- RN License
- 401(k)
14d
Canning Line Associate (WIP)
Wild Leaf Holdings U.S. LLC —Baltimore, MD
- $18 an hour
- Full-time
- Forklift
- High school diploma or GED
- Entry level
- Health insurance
- Paid time off
Quick Apply

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Associate II, Manufacturing

Catalent -
Harmans, MD

Apply Now

Job Details

Full-time
$31.25 - $36.05 an hour
10 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
Benefits from day one

Qualifications

Regulatory compliance
Good documentation practices (GDP)
English
Manufacturing standard operating procedures
Manufacturing facility experience
Records management
Quality control documentation
Quality assurance standard operating procedures
Laboratory standard operating procedures
Compliance documentation
Batch records
Collaboration with manufacturing teams
Standard operating procedures (SOPs)
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Associate II, Manufacturing

About Site

Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.

The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.

The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.

Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.

Position Summary

We have an opportunity for an Associate II, Manufacturing to join our team. In this role, you will support GMP upstream or downstream manufacturing processes for bulk biologics from microbial and cell culture systems. You will apply your knowledge to solve operational and routine tasks for Phase I/II and commercial GMP manufacturing. This position reports to the Supervisor, Manufacturing and plays a key role in ensuring compliance and operational excellence.

Shift: Day shift, 7am-7pm on a 2-2-3 rotation
Location: Harmans, MD - BWI
100% Onsite

The Role

Complete Batch Production Records under current Good Manufacturing Practices and document processes using Standard Operating Procedures and Batch Production Records
Generate operational protocols and internal or external documents including Standard Operating Procedures, Batch Production Records, deviations, and summary reports
Collaborate with Process Development and Manufacturing Sciences and Technology teams to transfer new projects into GMP
Generate and revise internal and external documents such as Standard Operating Procedures and Batch Records
Support initiation and closure of deviations; may lead departmental investigations and close deviations and Corrective and Preventive Actions
Troubleshoot process and equipment issues; work with Facilities and Validation to maintain manufacturing equipment
Recommend equipment and supply purchases for production areas
Develop creative solutions to operational problems using knowledge of available theories and proven solutions
Work closely with production management on current and new manufacturing projects to develop processes and techniques to meet objectives and avoid delays
Collaborate with various departments and assist other teams as needed
Interact with clients during manufacturing campaigns; may oversee and escort person-in-plant during campaigns
Participate in facility expansion and equipment validation activities
Maintain full training in all GMP manufacturing operations and documentation while adhering to safety guidelines
Perform other duties as assigned

The Candidate

Minimum Requirements

High School diploma or General Education Diploma with 4+ years of experience in upstream (fermentation/bioreactor) or downstream (column chromatography, buffer/media skid) biologic production processes under GMP compliance OR Associate’s degree in a Scientific, Engineering, or Biotech field with 2+ years of experience in upstream or downstream biologic production processes under GMP compliance OR Bachelor’s degree in a Scientific, Engineering, or Biotech field with 1+ years of experience in upstream or downstream biologic production processes under GMP compliance
Strong knowledge and ability to apply scientific principles to solve operational and routine production tasks
Excellent documentation skills including comprehension, review, and establishing Batch Production Records, Standard Operating Procedures, deviations, and summary reports
Team-oriented with the ability to collaborate effectively across Manufacturing, Quality Control, Quality Assurance, Regulatory, and Materials Management functions.
Strong written and verbal communication skills with proficiency in English.
Ability to work flexible schedules, including shift, overtime, and weekend coverage as required by production needs.
Capable of performing physical requirements of the role, including lifting up to 40 pounds and extended periods of standing, walking, bending, reaching, pushing, and pulling.
Ability to work safely and effectively in a manufacturing environment while maintaining a strong focus on quality, compliance, and operational excellence.

Pay

The anticipated hourly rate for this position in MD is $31.25 – $36.05 Plus Bonus. The final hourly rate offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why You Should Join Catalent

Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
Competitive paid time off plus 8 paid holidays
Community engagement and green initiatives
Medical, dental, and vision benefits effective day one of employment
Tuition Reimbursement

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Apply Now

Refine Your Search

senior manufacturing associate jobs in elkridge, md

Associate II, Manufacturing

Associate I, Manufacturing

Senior Associate Attorney

Senior Registered Client Service Associate - Hunt Valley, MD

Community Health Worker [Senior Associate] - Maryland

Research Associate, Assay V&V and Reagent Manufacturing Scale-Up

Associate Producer, Photo and Video

Associate, Strategic Marketing

Senior Accounting Associate, Aerospace, Defense, and Government

Sr. Clinical Research Associate

Associate - Quality Control

Business Development Sr. Associate

Senior Associate Appraiser

Sr Development Associate

Production Associate - HV

Operations Associate

Senior Associate, Clinical Trials & Corporate Contracts

Sr Associate Product Manager

Associate Healthcare Director/Assistant Director of Nursing

Canning Line Associate (WIP)

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Associate II, Manufacturing

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