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Dp Positions Jobs in Raleigh, NC (NOW HIRING)

Cellectis

Director, Quality Control

Raleigh, NC · On-site

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing ...

Cellectis

Director, Quality Control

Raleigh, NC

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing ...

Cellectis Group

Director, Quality Control

Raleigh, NC · On-site

$120 - $150/hr

POSITION RESPONSIBILITIES Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.

Fujifilm

Tech 2, Maintenance-DPFG

Holly Springs, NC

Position Overview The Technician 2, Maintenance for Drug Product Finished Goods (DPFG) is responsible for the installation, maintenance, and repair of Drug Product (DP) related systems/equipment (e.g ...

Fujifilm

Tech 2, Maintenance-DPFG

Holly Springs, NC · On-site

Position Overview The Technician 2, Maintenance for Drug Product Finished Goods (DPFG) is responsible for the installation, maintenance, and repair of Drug Product (DP) related systems/equipment (e.g ...

MSD

Director, Supply Chain Management

Durham, NC · On-site

$175K - $199K/yr

This Director (M3) level position as the Planning Lead for HPV Franchise leads a team of 5-6 supply ... Key activities include connecting the various nodes of the supply chain, engaging sites and DS/DP ...

Fujifilm

Analyst 1, QC Chemistry

Holly Springs, NC · On-site

Position Overview The Analyst 1, QC Chemistry works with direction to execute QC Analytical ... Ensures analytical testing of in-process, drug substance (DS), drug product (DP), and stability ...

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How much do dp positions jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for dp positions in Raleigh, NC is $15.45, according to ZipRecruiter salary data. Most workers in this role earn between $13.32 and $17.07 per hour, depending on experience, location, and employer.

What is a DP position?

DP positions, also known as Dynamic Positioning positions, refer to specialized roles in the maritime industry that involve operating and managing a vessel's dynamic positioning system. Dynamic positioning is a computer-controlled system that automatically maintains a ship's position and heading by using its own propellers and thrusters. People working in DP positions, like DP Operators or DP Officers, are responsible for ensuring the vessel remains steady, especially during sensitive operations such as drilling, diving, or loading cargo at sea. These roles require specialized training and certification to operate the DP systems safely and efficiently.

What are the key skills and qualifications needed to thrive as a Director of Photography (DP), and why are they important?

To thrive as a Director of Photography (DP), you need a strong understanding of cinematography, lighting techniques, camera operation, and visual storytelling, typically supported by a film degree or extensive on-set experience. Proficiency with camera systems (such as ARRI or RED), lighting equipment, and editing software like DaVinci Resolve is commonly required. Creativity, strong communication, leadership, and the ability to collaborate closely with directors and crew are standout soft skills. These combined abilities ensure the visual quality, consistency, and narrative impact of a film or video production.

What are some common challenges faced by Directors of Photography (DP) on set, and how can they be addressed?

Directors of Photography often encounter challenges such as managing tight shooting schedules, adapting to changing lighting conditions, and translating the director's vision into effective visual storytelling. Collaboration and clear communication with the director, camera crew, and lighting team are essential to overcome these hurdles. Staying flexible and prepared with backup plans for equipment or weather issues can also help DPs maintain productivity and creativity on set.

What is the difference between Dp Positions vs Video Editor?

AspectDp PositionsVideo Editor
Primary RoleResponsible for camera operation, lighting, and shot composition on setFocuses on editing footage, color correction, and post-production effects
Required SkillsCamera operation, lighting setup, shot framingEditing software proficiency, storytelling, color grading
Work EnvironmentOn-set, production locationsPost-production studios or editing suites
Common UsageFilm, TV, commercial shootsPost-production editing for various media

While Dp Positions focus on capturing footage during production, Video Editors work primarily in post-production to assemble and refine the footage. Both roles are essential in the filmmaking process but differ in responsibilities, skills, and work environment.

What are popular job titles related to Dp Positions jobs in Raleigh, NC?

For Dp Positions jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Dp Positions jobs in Raleigh, NC look for?

The top searched job categories for Dp Positions jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Dp Positions jobs?

Cities near Raleigh, NC with the most Dp Positions job openings:

Dp Positions jobs near you

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Re-posted 15 days ago

Job description


POSITION SUMMARY
The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site. This role is accountable for ensuing the generation of accurate, reliable, and compliant analytical data to support product release, stability, and lifecycle management in accordance with global GMP requirements.
The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.
POSITION RESPONSIBILITIES
  • Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.
  • Partner with AS&T to ensure the robustness and lifecycle management of the analytical control strategy including method qualification, validation, transfer, and performance monitoring.
  • Oversee analytical, microbiological, and environmental monitoring programs, ensuring compliance with GMP requirements and site contamination control strategy
  • Ensure data integrity, accuracy, and reliability of all QC data in accordance with regulatory expectations.
  • Establish and maintain inspection readiness, including hosting regulatory inspections and responding to health authority inquiries.
  • Drive timely and thorough investigations of OOS, OOT, and atypical results, ensuring appropriate root cause identification and effective CAPA implementation.
  • Ensure appropriate specifications, test methods, and acceptance criteria are established and maintained throughout the product lifecycle.
  • Oversee QC laboratory operations including resource planning, capacity management, and organizational capability development
  • Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support batch release, process improvements, and regulatory submissions.
  • Lead continuous improvement initiatives to enhance laboratory efficiency, compliance, and right-first-time performance.
  • Develop and monitor QC performance metrics, identifying trends and driving actions to improve performance and compliance.
  • Build and develop a high performing QC organization, fostering a strong quality culture and technical excellence.
  • Participates in business sub-teams as a Subject Matter Expert (SME) to provide input on timeliness and to address analytical/microbiological related issues
  • Other responsibilities and duties as the company may from time-to-time assign

EDUCATION AND EXPERIENCE
  • Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred.
  • Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles.
  • Strong leadership skills with experience building and leading high-performing technical teams.
  • Experience managing environmental monitoring and contamination control strategies in GMP manufacturing environments.
  • Experience supporting DS & DP manufacturing in GMP environments.
  • Proven track record of regulatory inspection success and audit management.
  • Proven experience with laboratory method lifecycle management.
  • Experience implementing or optimizing laboratory systems and processes preferred.

TECHNICAL SKILLS / CORE COMPETENCIES
  • Deep expertise in GMP regulations applicable to QC laboratories supporting ATMPs.
  • Strong knowledge of analytical techniques (e.g. q/rt/ddPCR, flow cytometry, ELISA, cell-based assays, microbiological methods) and their application tin DS/DP testing.
  • Strong understanding of data integrity principles and regulatory expectations (ALCOA+).
  • Ability to operate effectively in a matrixed, cross-functional environment.
  • Strong problem-solving skills with a risk-based and science-driven approach.
  • Excellent communication skills with the ability to influence at site and executive levels.
  • Strong project management skills.

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