ZipRecruiter

Log In

1

Associate Director Packaging Jobs in Rolesville, NC

MSD

Associate Director, Supply Chain Management

Durham, NC · On-site

$175K - $199K/yr

... inventory management, packaging, and delivery. In partnership with Marketing, Finance, and ... As a member of the Global Launch Planning (GLP) department, the Associate Director, Supply Chain ...

RSM

Solutions Architecture Associate Director

Raleigh, NC · On-site

$61.25 - $80.75/hr

Architecture Review At RSM, we offer a competitive benefits and compensation package for all our ... The salary range (or starting rate for interns and associates) for this role represents numerous ...

RSM

Solutions Architecture Associate Director

Raleigh, NC

$61.25 - $80.75/hr

Architecture Review At RSM, we offer a competitive benefits and compensation package for all our ... The salary range (or starting rate for interns and associates) for this role represents numerous ...

Novartis

QA Operations Head (Associate Director)

Durham, NC · On-site

$138K - $257K/yr

Minimum 8-10 years of relevant pharmaceutical experience including direct experience in oral solid ... US-based eligible employees will receive a comprehensive benefits package that includes health ...

next page

Showing results 1-20

All JobsAssociate Packaging JobsAssociate Director Packaging JobsAssociate Director Packaging Jobs in Rolesville, NC

Associate Director Packaging information

See Rolesville, NC salary details

$7

$11

$13

How much do associate director packaging jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for associate director packaging in Rolesville, NC is $11.41, according to ZipRecruiter salary data. Most workers in this role earn between $9.71 and $11.97 per hour, depending on experience, location, and employer.

Associate Director, Packaging Equipment Technology Engineering

Durham, NC • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 11 days ago

Job description

Responsibilities
  • Lead/support complex technical projects and equipment technology assessments in packaging and Medical Devices & Combination Products (MDCP) for new product introduction and product/device component source changes.
  • Lead/support global and site-centric capital/equipment projects: new packaging equipment purchases, equipment transfer/relocation, device component source change assessments, and packaging site operational/launch support.
  • Serve as the above-site packaging and assembly equipment SME for troubleshooting and equipment/end-to-end line performance & technology analysis.
  • Apply packaging technical/scientific concepts (mechanical/electrical knowledge, automation, AutoCAD/SolidWorks, equipment validation/qualification, Lean/Six Sigma, GMP, safety standards, project management, preventive/predictive maintenance, serialization, VOC, process capability, root cause analysis) to resolve technical issues.
  • Partner with Serialization CoE to implement, monitor, and troubleshoot serialization strategy.
  • Establish/maintain packaging equipment specification standards across multiple platforms.
  • Evaluate new technologies for compatibility with existing packaging lines and align with site technology groups.
QualificationsRequired
  • Bachelor's in Packaging Science/Engineering, Mechanical Engineering, or related discipline.
  • 10+ years in pharmaceutical/biotech/medical device industry; 3+ years in a leadership role (maintenance, operations, and/or engineering).
  • Experience developing/implementing equipment standards across multiple manufacturing/packaging sites.
  • Strong background in medical device/combination product/pharmaceutical packaging equipment and operations.
  • Experience from design control through product and technology transfer for new and existing facilities.
  • Exceptional project management skills.
  • Strong GMP/quality systems expertise: equipment/process qualification & validation, RCA, change control, deviation management, cleaning qualification.
  • Quantitative tools for RCA, risk management, and options analysis.
  • Knowledge of cGMP, FDA, EMA, and international regulatory requirements.
  • Strong analytical and communication skills.
Preferred
  • Advanced practical knowledge of packaging and device assembly equipment/processes.
  • Autonomous operation with strong coordination/communication/supervision.
  • Proven track record in fast-paced, compliant technical issue resolution.
#J-18808-Ljbffr

Apply