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求人Beam Therapeutics

Senior Manager, Quality Control Raw Materials

Beam Therapeutics

Senior Manager, Quality Control Raw Materials

Beam Therapeutics

Durham, NC

·

On-site

·

Full-time

·

Today

Company Overview:

Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.

Position Overview:

The QC Manager, Raw Materials will be responsible for developing, leading, and managing the Raw Materials QC program at the Beam Therapeutics Manufacturing facility in Durham, NC. This role will develop and maintain documentation regarding testing requirements and strategies, serve as a subject matter expert (SME) for raw materials issues, providing technical expertise aligned with current GMPs and current industry practices. This person will have knowledge and experience with USP methods, and the ability to apply as required, and as well as maintaining compliance to USP, ICH and FDA guidance documents. Interface with Manufacturing, Supply Chain, and Quality Assurance leadership and participate and/or lead interdepartmental teams to address quality-related issues.

This role requires on-site presence and engagement. The position will report to the Quality Control Senior Director.

Primary Responsibilities:

  • Build and manage the raw materials QC program at the Beam Therapeutics Manufacturing facility.
  • Develop and maintain all documentation with regards to testing requirements and strategies, including material specifications.
  • Serve as a SME for raw materials issues, providing technical expertise aligned with current GMPs and current industry best practices.
  • Manage contract laboratories as needed.
  • Own and author risk assessments for raw material programs.
  • Support supplier change notifications and material enrollment.
  • Identify need for development of new assays with compendial and GxP requirements.
  • Accountable for managing the raw materials testing program to ensure quality, product specifications and adherence to all current GMPs, USP, ICH and FDA guidance documents.
  • Evaluate QC systems and recommend and/or implement system improvements.
  • Author technical protocols and reports for Raw Materials testing qualification, validation, or verification.
  • Author test methods and SOPs for the Raw Materials testing program.
  • Create, review, and approve out-of-specification (OOS) and out-of-trend (OOT) investigations, deviations, CAPAs, and Change Controls.
  • Manages release of raw materials used in manufacturing.
  • Provide oversight of material master data as it relates to inspection plans and material life cycle.
  • Maintain records and databases in accordance with procedures.
  • Hire and manage staff as needed.
  • Oversee management of in-house raw material test equipment.

Qualifications:

  • Bachelor’s or advanced degree in biology, biochemistry or closely related scientific discipline.
  • At least 7-10 years of CGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • Expert knowledge of pharmaceutical/biotech Raw Materials testing is required.
  • At least 3 years of management experience is required.
  • Basic knowledge of qualifications and validations; current industry practices; and strong experience with guidance interpretation and application.
  • Knowledge of cGMPs, ICH, USP, FDA requirements is required, including equipment and method validation/verification.
  • Experience with risk assessment tools is desired
  • Excellent critical thinking and technical writing skills.
  • Excellent interpersonal and communication skills to lead, facilitate and follow.
  • Computer skills required to use Microsoft Word, Project, Visio, and Excel programs.

The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.

Beam Pay Range:

$155,000—$190,000 USD

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Beam Therapeuticsについて

Beam Therapeutics

Beam Therapeutics Inc. is an American biotechnology company conducting research in the field of gene therapies and genome editing. The company is headquartered in Cambridge, Massachusetts.

201-500

従業員数

Cambridge

本社所在地

$1.3B

企業価値

レビュー

3.7

10件のレビュー

ワークライフバランス

3.2

報酬

3.8

企業文化

4.1

キャリア

2.8

経営陣

3.9

65%

友人に勧める

良い点

Supportive and approachable management

Flexible working hours and remote work options

Great team culture and collaborative environment

改善点

Heavy workload and frequent overtime

High expectations leading to stress and burnout

Limited career advancement opportunities

給与レンジ

52件のデータ

Director

Director · Senior Director, Pharmacovigilance

1件のレポート

$172,500

年収総額

基本給

$150,000

ストック

-

ボーナス

-

$172,500

$172,500

面接体験

64件の面接

難易度

3.4

/ 5

期間

14-28週間

内定率

37%

体験

ポジティブ 64%

普通 19%

ネガティブ 17%

面接プロセス

1

Phone Screen

2

Technical Interview

3

System Design

4

Behavioral

5

Team Fit

よくある質問

Tell me about a challenging project

System design question

Coding problem

Why this company