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Director Cdmo Jobs in Georgia (NOW HIRING)

... CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire ...

Director Cdmo information

What is the difference between Director Cdmo vs Director Regulatory Affairs?

AspectDirector CdmoDirector Regulatory Affairs
Required CredentialsAdvanced degree in life sciences, engineering, or related field; industry experienceAdvanced degree in life sciences, law, or related field; regulatory certifications often preferred
Work EnvironmentContract manufacturing organizations, pharmaceutical or biotech companiesPharmaceutical companies, biotech firms, regulatory agencies
Employer & Industry UsageUsed in contract manufacturing and development settingsUsed in companies overseeing product approval and compliance

The main difference is that a Director Cdmo focuses on managing contract manufacturing and development projects, while a Director Regulatory Affairs handles regulatory compliance and approval processes. Both roles require advanced degrees and industry experience but serve different functions within the pharmaceutical and biotech sectors.

What are the most commonly searched types of Cdmo jobs in Georgia?

The most popular types of Cdmo jobs in Georgia are:

What job categories do people searching Director Cdmo jobs in Georgia look for?

The top searched job categories for Director Cdmo jobs in Georgia are:

Warehouse Associate

Atlanta, GA • On-site

$22/hr

Other

Posted 19 days ago


Job description

Warehouse Associate
Location: Marietta, GA
Industry: Pharmaceutical
Hours: 6am-2:30pm with mandatory OT and possible weekends (one could be required to come in later, stay later, etc. so need to be flexible with schedule).
Salary: Up to $22/hr.
Employment Type: Contract with the possibility to go perm (depends on client needs, performance, attendance, etc.)
Environment:
Client is a fully integrated biopharmaceutical company focused on developing, manufacturing and commercializing specialty products. Our diversified product portfolio in the specialty neurology and women's health space, together with our non-promoted complex formulations of generic drugs, form the foundation of our unwavering commitment to improve patients' lives.
Description
Coordinates the flow of raw materials and finished product through the warehouse and manufacturing areas.
Essential Responsibilities:
  • Receives incoming inventory items, verifies accuracy against PO, generates and applies batch labels, stocks inventory in the proper location and maintains the item receiving paperwork.
  • Move materials physically and within ERP Computer System to storage areas and ERP Computer System areas.
  • Create Journals (Movement, Transfer, Adjustment) as required and maintain appropriate paperwork.
  • Manage and process production and DEA waste area
  • Responsible for outbound shipping, included packing, labeling and shipping.
  • Maintain all assigned training compliance.
  • Submit/Maintain all documentation in accordance with good manufacturing practices and all applicable SOPs.
  • Performs cycle counts and inventory as required
  • Interact in a professional manner with internal and external customers
  • Monitor production schedule and anticipate production support requirements.
  • Any other activities to support the Marietta site
Core Competencies
  • Demonstrates characteristics of a good team member
  • Initiative to help without direct supervisor or lead direction.
  • Contributes fair share of the work.
  • Maintains good performance standards.
  • Works assigned shifts and stays to complete as needed to support production demands
  • Prepares materials for next batch or process
  • Maintains good attendance standards.
  • Maintain GMP Compliance.
  • Complies will all Safety Policies and consistently performs duties safety.
Minimum Qualifications
  • High School Diploma (or equivalent) or technical school certificate
  • 1 -2 years Warehouse experience.
  • Familiarity with Microsoft Office applications required.
  • Experience with SAP is highly desirable.
  • Previous experience working in a regulated environment (GMP or FDA; preferred)
  • Steel toed boots required.
Physical Requirements
  • Must be able to bend repeatedly and lift up to 50 lbs.
  • Must be able to be on feet extended periods of time
EOE/ADA
SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model-partnering closely with clients to understand not only the role, but the company's culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.