Specialist, Quality Document Control

Specialist, Quality Document Control Cranbury, NJ Job Details Full-time $56,000 - $74,000 a year 2 days ago Benefits Paid holidays Health insurance Dental insurance Vision insurance 401(k) matching Life insurance Qualifications Productivity software Associate's degree

Full Job Description Overview:

Create a future where DNA is no longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We are a team of creative, compassionate, and driven individuals united by a profound mission of seeking gene therapy cures. Rocket places tremendous value on our people and fosters a collaborative environment where bold ideas thrive and every team member makes a meaningful impact. Our core values guide everything we do: we trust one another, show generosity toward patients, embrace curiosity, and strive to elevate science. Team members receive a competitive total rewards package, including equity participation, 401(k) matching, and excellent health benefits.

Position Summary:

The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system. This role will manage all paper-based documents and records and will be the primary owner of the document control storage room that houses all paper records/logbooks, batch records, etc.

Responsibilities:

Management of documents within the ZenQMS electronic quality system. Issuance and archiving of all paper-based documents and records, including batch records, logbooks, controlled forms, etc. Oversight and management of the on-site physical document storage room Support the various functional groups in managing their documents Supporting the ZenQMS team in managing documents within the system

Qualifications:

Associates Degree Minimum three years of experience in a document control or document management role Experience with electronic document management systems (ZenQMS, Veeva, etc.) Minimum of 3-5 years of quality biopharma experience Familiar with standard software systems (Microsoft Word, Excel, PowerPoint, etc.) Ability to work within a multifunctional team Degree in science related field preferredWork with documents, pushing carts to transport batch records and large sets of documents/binders

Compensation:

The expected salary range for this position is $56,000 to $68,000. At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee's experience, location of the position and availability of similar talent in a competitive market. For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts. In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year's, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives).

EEO Statement:

A diverse workforce fosters innovation and strengthens Rocket's business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws.