Quality Specialist - cGMP Manufacturing - 3rd Shift

Alcami Corporation•Charleston, SC

8d•Onsite

About The Position

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Quality Specialist will provide site quality support in a fast-paced environment by effectively performing activities of substantial variety to ensure quality and compliance with applicable regulatory requirements and is proficient in all document and protocol approvals applicable to the respective processes executed at the respective lab or manufacturing facility. Activities include reviewing documents and data, supporting audits and inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The position develops SOPs or other quality documents as needed. On-Site Expectations 100% on-site position. 3rd Shift: Sunday - Thursday, 11:00pm - 7:30am.

Requirements

Bachelor’s degree in Chemistry, Biology, or relevant field and 3+ years of related experience required, or Master’s degree in relevant field and 1+ years of related experience.
Relevant GMP experience required.
Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise.
Good written and oral communication skills.
Good math skills.
Good computer skills and knowledge of Microsoft Office products.
Ability to be trained and to mentor.
Ability to act independently.
Ability to interact well with clients and regulatory agents.
Ability to negotiate.
Ability to interact well with employees at all levels.
Ability to act as technical consultant.
Uses professional concepts and company policies and SOPs to solve a variety of problems.
Receives minimal instruction on day-to-day work, general instructions on new assignments.

Nice To Haves

Experience in Environmental monitoring and critical utilities preferred for sterile operations.

Responsibilities

Performs quality review and approval of complex documents, all types of data, protocols, and/or reports.
Supports quality floor audits and/or floor inspections.
Supports for client and regulatory agency audits and inspections.
Provides quality evaluation and release of support materials, products, equipment and facilities as required.
Maintains quality databases and may perform analysis and trending.
Assists with quality improvement initiatives as needed.
Develops quality SOPs or other quality documents and/or reports as needed.
Provides consultation on complex quality and compliance topics in areas of expertise.
Develops and provides training in quality and compliance topics in areas of expertise.
Provides Quality oversite for the site specific Quality Management Systems including Investigations, Corrective Actions, Change control, etc.
Effectively performs a variety of complex duties, on schedule, with accuracy and competency.
Maintains accurate files and records.
Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
Other duties as assigned.