Cmc Medical Writer

Canton, MI, United States

Job Description


MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO in Global Health & Pharma\xe2\x80\x99s international awards programs for the last three consecutive years. For more information, visit or follow MMS on .

Roles & Responsibilities:

  • Experience with development and writing of CMC-related documents (Module 2.3 QOS and Module 3: 3.2.S, 3.2.P, 3.2.A, 3.2.R)
  • Strong understanding of regulatory guidances as it applies to CMC submissions (eg, NDAs, MAAs, BLAs, INDs, IMPDs)
  • Interpret and analyze quality data related to product characterization, manufacturing process, product and process control, and stability
  • Organizational expert within the CMC subject area
  • Ability to complete documents according to sponsor\'s format, processes, and according to regulatory guidelines
  • Lead projects independently with minimal oversight
  • Interpret and analyze applicable CMC data
  • Collaborate with cross-functional teams such as safety, nonclinical, clinical, QC, publishing
  • Demonstrated ability to lead others to complete complex projects
  • Ability to complete documents according to sponsor\xe2\x80\x99s format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings
Requirements:
  • BS + in biology or chemistry, or related field, with industry experience within regulatory affairs, laboratory sciences, quality assurance/control
  • Knowledge of GMP, ICH guidelines, and applicable regulatory requirements
  • 2+ years of pharmaceutical regulatory CMC writing experience
  • Strong writing and analytical skills
Powered by JazzHR

MMS Holdings

Beware of fraud agents! do not pay money to get a job

MNCJobz.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.


Related Jobs

Job Detail

  • Job Id
    JD4318697
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Canton, MI, United States
  • Education
    Not mentioned