ZipRecruiter

Log In

1

Bmram Jobs in Virginia (NOW HIRING)

Granules

Operations Associate

Chantilly, VA · On-site

Manage master data by creating new records, editing the records and generating reports in Blue Mountain Regulatory Asset Manager (BMRAM) software. * Assist in pharmaceutical environment handling DEA ...

All JobsBmram JobsBmram Jobs in Virginia

Bmram information

What is a BMRAM?

BMRAM stands for Biased Magnetoresistive Random Access Memory, a type of non-volatile memory technology used in computing. Unlike traditional RAM, BMRAM retains data even when power is turned off, making it useful for data storage and memory applications that require persistence. The technology leverages magnetic properties to store information, potentially offering faster speeds and greater durability compared to some other non-volatile memory types. BMRAM is still an emerging technology, with ongoing research aimed at improving its efficiency and scalability.

What are the key skills and qualifications needed to thrive as a BMRAM, and why are they important?

To thrive as a BMRAM, you need strong analytical skills, risk assessment expertise, and a background in finance, mathematics, or a related field, often supported by relevant degrees or certifications. Familiarity with risk modeling software, statistical analysis tools, and regulatory compliance systems is typically required. Exceptional communication, problem-solving abilities, and attention to detail help professionals excel in collaborating with stakeholders and interpreting complex data. These skills are crucial for identifying, managing, and mitigating financial risks to ensure organizational stability and compliance.

What are the most common challenges faced by BMRAMs when aligning risk management strategies with business objectives?

One of the main challenges BMRAMs encounter is ensuring that risk management initiatives are closely integrated with the organization's overall business objectives, rather than being seen as separate compliance activities. This requires effective communication and collaboration across departments, as well as the ability to translate complex risk data into actionable insights for business leaders. BMRAMs must also stay current with regulatory changes and industry best practices to anticipate potential risks. Building strong relationships with stakeholders helps in promoting a risk-aware culture and achieving alignment between risk mitigation and business goals.

What is the difference between Bmram vs Bmram?

AspectBmramRelated Job Title
Required CertificationsTypically requires specific Bmram certifications or trainingMay require similar certifications, but often less specialized
Work EnvironmentPrimarily in manufacturing, industrial, or technical settingsSimilar environments, often overlapping in industrial sectors
Industry UsageCommonly used in sectors like manufacturing, engineering, or technical servicesUsed in related fields such as technical support or maintenance
Search & Comparison IntentPeople compare Bmram with similar technical roles to understand qualifications and dutiesOften searched together due to overlapping responsibilities

The comparison between Bmram and related technical roles highlights similarities in certifications and work environments. Both roles are prevalent in industrial sectors and often require specialized training. Understanding these differences helps job seekers identify the right career path and employers find suitable candidates more efficiently.

What are popular job titles related to Bmram jobs in Virginia?

For Bmram jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Bmram jobs in Virginia look for?

The top searched job categories for Bmram jobs in Virginia are:

What cities in Virginia are hiring for Bmram jobs?

Cities in Virginia with the most Bmram job openings:

Bmram jobs near you
Infographic showing various Bmram job openings in Virginia as of August 2026, with employment types broken down into 67% Full Time, 15% Part Time, and 18% Contract. Highlights an 100% Physical job distribution.

Operations Associate

Granules

Chantilly, VA • On-site

Full-time

Posted 9 days ago

Job description

Description:

The Operations Associate plays a key role in ensuring the smooth and compliant operation of both warehouse and manufacturing processes. This position is responsible for a wide range of duties, including maintaining cGMP standards, supporting material movement and inventory control, and overseeing the preparation and review of essential documentation. The associate will also actively engage with SAP for master data management, assist in the implementation of automation initiatives, and participate in the validation of GMP equipment. Additionally, this role involves collaboration across teams, ensuring the accuracy of reports, managing operational improvements, and maintaining rigorous adherence to regulatory requirements. With a focus on precision, process optimization, and compliance, the Operations Associate will contribute to the overall efficiency and quality of manufacturing operations. Personnel should perform function in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.


Responsibilities:

  • Maintain awareness of new and emerging computational methods and technologies (Data analysis) for inventory control.
  • Participate in the preparation of cycle count reports and periodic publication.
  • Document all changes, modifications, or issues in the database using the change control program.
  • Creating and maintaining the master data in SAP (BOM master, Resource master, Production version, Material master, Inspection plan etc.).
  • Engage as a user in managing SAP in inventory control.
  • Develop skills and provide user support for PP/MM modules in SAP.
  • Use computer sequential process for querying databases.
  • Create data management or error checking procedures including corrective actions
  • Actively participate in implementing and enhancing automation in manufacturing activities.
  • Participate in Computer system validation activities for the equipment involved in GMP (IQ/OQ/PQ).
  • Analyze data reports like stock statement, production report, consumption report and shipments etc.
  • Manage master data by creating new records, editing the records and generating reports in Blue Mountain Regulatory Asset Manager (BMRAM) software.
  • Assist in pharmaceutical environment handling DEA materials and Data entry and perform activities for various materials received.
  • Write, revise, and review of SOP’s that are related to job functions.
  • Creates purchase requisitions for the acquisition of materials for manufacturing
  • Participating in operational, safety, quality and management initiatives.
  • Perform Any other activity as assigned by the Supervisor.
Requirements:
  • A background in cGMP compliance and DEA compliance within the pharmaceutical manufacturing industry is required.
  • Experience in writing and maintaining cGMP documentation.
  • Experience in materials receipt and storage.
  • Ability to analyze data/information and to assess and resolve complex issues, as required.
  • Good verbal and written communication skills are required.
  • Ability to work and communicate with cross-functional teams.
  • Ability to manage multiple priorities and re-prioritize tasks, as required.
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Strong attention to detail and excellent organization.

Education/Experience:

  • Degree: Minimum Bachelor’s degree; a degree in Healthcare informatics, or any scientific discipline.
  • Experience: 2+ years of experience in a cGMP-regulated environment, with experience in pharmaceutical manufacturing highly preferred.

Disclaimer:

The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.